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. 2014 Jun 2;5:250. doi: 10.3389/fimmu.2014.00250

Immunologic Basis for Long HCDR3s in Broadly Neutralizing Antibodies Against HIV-1

Lei Yu 1, Yongjun Guan 1,2,*
PMCID: PMC4040451  PMID: 24917864

Abstract

A large number of potent broadly neutralizing antibodies (bnAbs) against HIV-1 have been reported in recent years, raising hope for the possibility of an effective vaccine based on epitopes recognized by these protective antibodies. However, many of these bnAbs contain the long heavy chain complementarity-determining region 3 (HCDR3), which is viewed as an obstacle to the development of an HIV-1 vaccine targeting the bnAb responses. This mini-review summarizes the current literature and discusses the different potential immunologic mechanisms for generating long HCDR3, including D–D fusion, VH replacement, long N region addition, and skewed D–J gene usage, among which potential VH replacement products appear to be significant contributors. VH replacement occurs through recombinase activated gene-mediated secondary recombination and contributes to the diversified naïve B cell repertoire. During VH replacement, a short stretch of nucleotides from previously rearranged VH genes remains within the newly formed HCDR3, thus elongating its length. Accumulating evidence suggests that long HCDR3s are present in significant numbers in the human mature naïve B cell repertoire and are primarily generated by recombination during B cell development. These new observations indicate that long HCDR3s, though low in frequency, are a normal feature of the human antibody naïve repertoire and they appear to be selected to target conserved epitopes located in deep, partially obscured regions of the HIV-1 envelope trimer. Therefore, the presence of long HCDR3 sequences should not necessarily be viewed as an obstacle to the development of an HIV-1 vaccine based upon bnAb responses.

Keywords: VH replacement, HIV-1, broadly neutralizing antibodies, long HCDR3, immunologic mechanism, vaccines

Introduction

The development of a protective HIV-1 vaccine is believed to be the best hope in the battle against HIV-1/AIDS. However, this goal remains elusive after 30 years of intense effort. Broadly neutralizing antibodies (bnAbs) against the HIV-1 envelope protein (Env) can be protective, as shown by passive immunization studies in non-human primates and humanized-mouse models (1–11). However, no HIV-1 vaccine candidate has been able to elicit a bnAb response. In the last 5 years, many novel bnAbs have been identified and are actively being pursued as templates for the rational design of an effective HIV-1 vaccine (12–20). Understanding the immunologic basis for the generation of these bnAb should help the design of an effective HIV-1 vaccine.

HIV-1 Broadly Neutralizing Antibodies have Unique Features

Many potent bnAbs have been isolated and characterized from multiple subjects in the last 5 years (21–33), mainly due to the application of efficient methods for isolation of human monoclonal antibodies (mAbs) (27, 30, 34–37). These new HIV-1 bnAbs are much more potent and broader than previously described neutralizing Abs. With the elucidation of crystal structures of the HIV-1 Env trimer and gp120-antibody complexes (38–41), the vulnerable epitopes on the HIV-1 Env targeted by bnAbs are becoming clear. These new bnAbs can be categorized into four groups (Table 1). The first group is CD4 binding site (CD4bs) bnAbs represented by “VRC01-like” bnAbs (26, 28, 31, 32) that block Env binding to the primary receptor CD4. The second group includes the PGT series (29, 42–44), “PG9-like” bnAbs [PG9, PG16 (30), and CH01–04 (21)], which recognize both protein and glycan elements involving the V1V2 and V3 regions of gp120. The third group includes the recently described PGT151 series of bnAbs and the redefined 8ANC195 bnAb, which recognize glycan-related, gp120 and gp41 bridging regions (45–47). The fourth group targets the membrane-proximal external region (MPER) on gp41 and includes the antibodies 2F5, 4E10, 10E8, and M66.6 (24, 48, 49). These bnAbs collectively neutralize a majority of highly diverse HIV-1 strains. The new bnAbs and the recent crystal structure of HIV-1 Env trimer in complex with bnAbs have shed light on epitopes that could represent the basis for an Ab-based HIV-1 vaccine design. However, there are some common features of bnAbs that pose challenges to the development of a bnAb-based AIDS vaccine [reviewed in Ref. (20, 50) and Table 1].

Table 1.

Characteristics of the heavy chain V-gene of HIV-1 broadly neutralizing antibody.

Category based on epitope cluster HIV-1 bnAb
 Heavy chain genes
 HCDR3 (IMGT)
 VH somatic mutation
 Auto/poly reactivity**
Class Clone V gene D gene J gene Length Potential VH replacement* No. of nt (%) No. of AA (%)
CD4 binding site (CD4bs) b12 b12 IGHV1-3 D1-1 J6*03 20 No 35 (12.2) 20 (20.8) No
VRC01 3BNC117 IGHV1-2 D6-25 J6*04 12 Yes 75 (26.0) 34 (35.4) Yes
3BNC60 IGHV1-2 D3-3 J6*04 12 Yes 82 (28.5) 38 (39.6) Yes
PG19 IGHV1-2 D6-25 J1*01 13 ND 66 (22.9) 30 (31.3) NR
VRC01 IGHV1-2 D2-21 J2*01 14 Yes 91 (31.6) 40 (41.7) Neg.R
VRC02 IGHV1-2 D5-12 J2*01 14 Yes 92 (31.9) 38 (39.6) Neg.R
VRC23 IGHV1-2 D5-24 J4*02 14 ND 62 (21.5) 30 (31.3) NR
PG20 IGHV1-2 D3-10 J1*01 15 ND 69 (24.0) 36 (37.5) NR
12A12 IGHV1-2 D4-17 J2*01 15 No 64 (22.2) 33 (34.4) Yes
12A21 IGHV1-2 D1-26 J2*01 15 Yes 60 (20.8) 30 (31.3) Yes
CH30 IGHV1-2 D3-16 J4*02 15 Yes 69 (24.0) 37 (38.5) Neg.R
CH31 IGHV1-2 D5-12 J4*02 15 Yes 72 (25.0) 37 (38.5) Neg.R
VRC03 IGHV1-2 D2-21 J4*02 16 Yes 85 (29.5) 39 (40.6) Neg.R
VRC-PG04 IGHV1-2 D2-8 J2*01 16 No 84 (29.2) 42 (43.8) Neg.R
VRC-PG04b IGHV1-2 D2-15 J2*01 16 Yes 82 (28.5) 42 (43.8) Neg.R
VRC06 IGHV1-2 D2-21 J5*02 17 ND 88 (30.6) 46 (47.9) NR
NIH45-46 IGHV1-2 D1-26 J2*01 18 Yes 94 (32.6) 39 (40.6) Yes
3BC176 IGHV1-2 D5-12 J3*01 21 ND 69 (24.0) 34 (35.4) Yes
3BC315 IGHV1-2 D5-12 J3*01 21 ND 48 (16.7) 24 (25.0) Yes
8ANC131 8ANC131 IGHV1-46 D3-16 J6*01 18 No 74 (26.0) 38 (40.0) Yes
8ANC134 IGHV1-46 D3-16 J6*01 18 No 76 (26.7) 37 (38.9) Yes
1NC9 IGHV1-46 D5-24 J4*02 21 Yes 71 (24.7) 36 (37.5) Yes
1B2530 IGHV1-46 D3-10 J5*02 18 Yes 80 (27.8) 39 (40.6) Yes
CH103 CH103 IGHV4-61 D4-23 J4*01 15 ND 45 (15.8) 19 (20.0) Yes
Glycan-dependent, V1/V2 and V3 related (QNE/supersite) 2G12 2G12 IGHV3-21 D1-26 J3*01 16 ND 61 (21.2) 31 (32.3) Yes
PGT145 PGT145 IGHV1-8 D4-17 J6*02 33 Yes 48 (16.7) 27 (28.1) NR
PGT141 IGHV1-8 D4-17 J6*02 34 Yes 46 (16.0) 27 (28.1) NR
PGT142 IGHV1-8 D4-17 J6*02 34 Yes 47 (16.3) 29 (30.2) NR
PG9 CH01 IGHV3-20 D3-10 J2*01 26 Yes 48 (16.7) 28 (29.2) Neg.R
CH02 IGHV3-20 D3-10 J2*01 26 ND 41 (14.2) 22 (22.9) Neg.R
PG9 IGHV3-33 D3-3 J6*03 30 No 40 (15.1) 18 (18.9) Neg.R
PG16 IGHV3-33 D3-3 J6*03 30 No 43 (14.9) 21 (21.9) Neg.R
PGT128 PGT135 IGHV4-39 D3/OR15-3a J5*02 20 Yes 54 (18.6) 28 (28.9) NR
PGT137 IGHV4-39 D2-15 J5*02 20 Yes 67 (23.0) 32 (33.0) NR
PGT125 IGHV4-39 D3/OR15-3a J5*02 21 Yes 60 (20.6) 28 (28.9) NR
PGT127 IGHV4-39 D3-16 J5*02 21 Yes 46 (15.8) 25 (25.8) NR
PGT128 IGHV4-39 D3-10 J5*02 21 Yes 59 (20.3) 29 (29.9) NR
PGT121 PGT121 IGHV4-59 D3-3 J6*03 26 Yes 56 (19.6) 23 (24.2) NR
PGT122 IGHV4-59 D3-3 J6*03 26 Yes 56 (19.6) 25 (26.3) NR
10-1074 IGHV4-59 D3-3 J6*03 26 ND 45 (15.8) 20 (21.1) NR
VRC24 VRC24 IGHV4-4 D3-9 J5*02 26 ND 64 (22.5) 29 (30.2) NR
Glycan-related, gp120/gp41 bridging region 8ANC195 8ANC195 IGHV1-3 D3-3*01 J4*02 22 ND 80 (28.4) 40 (42.6) Yes
PGT151 PGT151 IGHV3-30* J6*02 28 ND 60 (20.8) 27 (28.1) Neg.R
PGT152 IGHV3-30 J6*02 28 ND 56 (19.6) 29 (30.2) Neg.R
PGT154 IGHV3-30 J6*02 28 ND 53 (18.4) 25 (26.0) NR
PGT158 IGHV3-30 J6*02 28 ND 61 (21.2) 30 (31.2) NR
gp41 MPER MPER 4E10 IGHV1-69 D1-1 J4*02 20 ND 19 (6.6) 18 (18.8) Yes
2F5 IGHV2-5 D3-3 J6*02 24 ND 41 (14.1) 14 (14.4) Yes
10E8 IGHV3-15 D3-3 J1*01 22 ND 63 (21.4) 26 (26.5) Neg.R
M66.6 IGHV5-51 D3-10 J6*02 23 ND 11 (3.8) 9 (9.4) Yes
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HIV-1 bnAb information was obtained from the Antibody Database, kindly provided by Dr. Anthony West (20) and the sequences were analyzed using IMGT V-QUEST (51).

*Potential VH replacement footprints were determined as reported (52). ND, not determined.

**Neg. R, negative in in vitro assay reported; NR, not reported. It should be noted that an in vivo test will be needed to determine a truly negative auto-/poly-reactivity as it was determined for b12. Although no direct auto-/poly-reactivity data for the PGT series bnAbs were reported, several representative antibodies of them (PGT121, PGT128, 10-1074, etc.) were shown to mediate effective protection in in vivo passive immunization studies, which indicates that they are likely negative in auto-/poly-reactivity.

The first is that the new HIV-1 bnAbs are highly somatically mutated, especially in the variable heavy chain region (VH) genes (21, 22, 26, 28–32, 53). This is in contrast with other human immunoglobulin G (IgG) antibodies and HIV-specific IgG antibodies with limited neutralizing activity (27, 54, 55). Many of the HIV-1 bnAbs also have insertions and deletions in their complementarity-determining regions (CDRs) (17, 26). This may reflect their prolonged, complex maturation path in vivo (17, 26, 56, 57), which would require extensive activity of activation-induced cytidine deaminase (AID) in germinal center B cells (58). Thus, induction of such highly somatically mutated antibody responses by vaccination is obviously a major challenge for bnAb-based HIV-1 vaccine development (20, 50).

The second feature is that many of the HIV-1 bnAbs are auto/poly reactive (26, 28, 31, 32, 59, 60). This might be a property acquired in the development of HIV-1 specific B cells during chronic HIV-1 infection that bypasses multiple B cell tolerance checkpoints (37, 61, 62). This phenomenon might be one of the reasons why a bnAb is usually generated after prolonged exposure to viral antigen in some HIV-1 infected people (26, 61, 62). Whether the auto/poly reactivity of these HIV-1 bnAbs is severe enough to prevent the induction of these antibodies in vivo in healthy individuals, which could be determined by in vivo testing of antibody gene knock-in animal models (63), will be critical to the success of a vaccine targeting these bnAbs (59). Alternatively, bnAbs with no or minimal auto/poly reactivity should be chosen as templates for HIV-1 vaccine (18, 24, 53, 61).

Another interesting feature is that many of the HIV-1 bnAbs have long (20–34 residues) heavy chain complementarity-determining region 3 (HCDR3) sequences (Table 1), especially in antibodies of the glycan-related V1/V2 and V3 category (Supersite group), the gp120/gp41 bridging region category and the gp41-MPER category. This contrasts with an average length of 16 residues of HCDR3 in human B cells (54). The HCDR3s of CD4bs bnAbs are relatively short (Table 1). The PG9-like and PGT128-like bnAbs in the Supersite group appear to have a long HCDR3 that can penetrate the glycan shield of the Env trimer and interact with the V1/V2 and/or V3 region of gp120. The new MPER targeting 10E8 also uses a long CDRH3 loop to reach the highly conserved hydrophobic residues on gp41 (42–44, 53). A bias against long HCDR3s during B cell development has been demonstrated in mice and rabbits (64, 65), which complicates using small animal species as an HIV-1 bnAb-based vaccination model (66). Although humans do generate antibodies with very long HCDR3s (67), the lower frequency of B cells encoding long HCDR3s and the potential bias of auto-reactivity were viewed as a challenge for eliciting bnAbs of long HCDR3s by vaccination due to the negative regulation of these antibodies during B cell development (14, 19, 37, 53, 64, 66). However, it should be noted that, although many long HCDR3 antibodies were reported to be auto-reactive and B cell precursors of auto-reactive antibodies are under negative selection during B cell development (37), the long HCDR3 and the auto-reactivity are two distinct aspects of antibodies. It is neither true that all long HCDR3 antibodies are auto-reactive, nor that all auto-reactive antibodies have long HCDR3s, though a long HCDR3 and auto-reactivity can sometimes be present in the same antibody. Data with HIV-1 bnAbs indicate that the negative selection against B cells encoding long HCDR3s is most likely a result of negative selection against auto-reactivity instead of the long HCDR3 itself. Many of the long HCDR3 bnAbs in the “Supersite” group of HIV-1 bnAbs and the PGT151 series bnAbs are not auto/poly reactive, while the CD4bs bnAbs group has many auto/poly reactive antibodies with shorter HCDR3s [Table 1 and review of (60)]. B cell precursors of non-auto-reactive long HCDR3 antibodies can pass negative selection checkpoints to become mature B cells. This view is strongly supported by the recent observation that long HCDR3s are present in significant numbers in the human naïve B cell repertoire and that they are primarily generated by the recombination events during B cell development (68).

Here, we review the current literature on the immunologic mechanisms for the generation of antibodies with long HCDR3s, among which potential VH replacement products appear to make a significant contribution in the generation of HIV-1 bnAbs. Our view is that, though negatively selected during B cell development, long HCDR3s are not necessarily an obstacle in the development of an HIV-1 vaccine targeting long HCDR3 bnAb responses.

Immunologic Mechanisms for Generating Antibodies with Long HCDR3

HCDR3, a key determinant of antibody specificity (69), is a product of combinatorial rearrangement of the variable (V), diversity (D), and joining (J) gene segments. It is composed of the sequence from the V–D junction, the D region, the D–J junction and the 5′ end of the J gene. The alternative use of D reading frames, variation in junction sites due to P-nucleotides and addition of N-nucleotides, in addition to VDJ recombination and somatic hypermutation (SHM), contribute to HCDR3 diversity (70, 71). Secondary mechanisms of receptor editing/revision, gene conversion, and VH replacement also contribute to the HCDR3 diversity (72–75). Among the diversities of HCDR3, the length of HCDR3 can have a large impact on the function of the antibody repertoire and varies from mouse to human (64, 65). Four immunologic mechanisms have been described that can increase the length of HCDR3.

Contribution of Somatic Hypermutation to Long HCDR3s

The accumulation of insertions introduced during the SHM process can theoretically increase the length of HCDR3 (76, 77). SHM related insertion/deletions (In/Dels) contribute substantially to the diversity of the human antibody repertoire, with an estimated frequency of 1.3–6.5% in circulating B cells, though short (1–2 residues) insertions are much more frequent than long insertions (77, 78). Interestingly, In/Dels from somatic mutation play a critical role in some bnAbs against HIV-1. The VRC01-like CH31-class bnAbs (Table 1) have a nine-residue insertion in H-CDR1 (32). The VRC06 bnAb has a seven-residue insertion in H-FR3 (33). The PGT128-class bnAbs have a 5–6 residue insertion in H-CDR2 (29). However, the contribution of SHM related insertion to long HCDR3s is hard to assign due to the complex nature of VDJ junctions. A convincing result from an in depth analysis of HCDR3 length by next-generation sequencing demonstrated that SHM typically does not alter the length of HCDR3 and long HCDR3s are not generated primarily through SHM related insertions (68).

Long HCDR3s Usually Arise during VDJ Recombination

B cell precursors with long HCDR3s tend to be auto-reactive and are negatively selected during B cell development, which is a recognized mechanism for the bias against long HCDR3s in human mature B cell repertoire (37). However, deep sequencing the human HCDR3 repertoire revealed that long HCDR3s are present in the mature naïve B cell repertoire at a significant frequency (68). The naïve B cell pool contains 3.5% B cells of HCDR3s ≥24 residues and 0.43% B cells of very long HCDR3s (≥28 residues). The features of P- and N-addition length from VDJ recombination show positive correlations with increasing HCDR3 length. Further, the B cells encoding long HCDRs display biased germline gene usage. Long HCDR3s show a strong association with the use of the D2 (D2-2 and D2-15) and D3 (D3-3) gene families and the use of J6 gene segment. Interestingly, many of the HIV-1 bnAbs with long HCDR3s use these preferred D and J gene segments. The PG9-class and PGT121-class bnAbs use the D3-3 and J6 gene segments and show very long HCDR3s (Table 1). It should be noted that these long HCDR3-associated human D and J gene segments are substantially longer than other D and J gene segments (68). Small animals such as mice and rabbits do not have similar long D and J gene segments, which might be why they do not generate antibodies with long HCDR3s and why small animal species are not considered suitable as HIV-1 bnAb-based vaccination models (66). This further supports the idea that long HCDR3s are established in humans primarily during VDJ recombination before the antigen-driven affinity maturation process.

D–D Fusion Recombinants Can Generate Long HCDR3s

D–D fusion is a V(DD)J recombination event that allows the generation of extremely long HCDR3s. D–D fusions are difficult to produce through normal V(D)J recombination because they violate the 12/23 rule (79). Although rare, these non-12/23 recombination events have been reported in in vitro and in vivo systems (80–82). High-throughput deep sequencing demonstrated that the frequency of D–D fusion in the naïve B cell population is about 1 in 800 naive B cells (79). The frequency is reduced in memory B cells. However, due to potential mismatches from somatic hypermutation, it is a challenge to accurately determine the frequency of D–D fusion in somatic-mutated memory B cells. The contribution of D–D fusion to long HCDR3s of HIV-1 bnAbs is unknown because almost all the bnAbs exhibit extensive hypermutation that make it hard to accurately match the germline D gene segments of HIV-1 bnAbs. HIV-1 bnAbs of PGT145 and PG9 classes (Table 1) have extremely long HCDR3s (34 and 30 residues, respectively) and are highly somatically mutated. IMGT junction analysis (51) of the HCDR3 of PGT145 reveals a 12 bp D4-17 sequence with three mismatches as well as an 11 bp D5-24 sequence with two mismatches, indicating that the long HCD3 of PGT145 might be the product of a D–D fusion. Therefore, it is possible that some HIV-1 bnAbs are derived from naïve B cells with D–D fusions.

VH Replacement Contributes Significantly to Long HCDR3

VH replacement is a well-recognized mechanism of antibody gene rearrangement (73, 83). It occurs through recombinase activated gene (RAG)-mediated secondary recombination (84) and contributes to the diversified naïve B cell repertoire (85). It is a process in which secondary V–V(D)J recombination results in replacement of the variable gene while preserving the original D–J recombination. It appears to occur early in B cell development as a mechanism to rescue non-functional and unwanted IgH genes to further diversify the IgH repertoire (86–88). The secondary recombination during VH replacement involves a cryptic recombination signal sequence (RSS) within a previously rearranged V(D)J joint with a 23 bp RSS from an upstream invading VH gene (86). During this process, a short stretch of nucleotides from previously rearranged VH genes are left within the newly formed HCDR3 and, therefore, elongate the HCDR3 region and provide a potentially identifiable “footprint” of VH replacement (75, 89).

By footprint analysis, the frequency of VH replacement in normal peripheral B cells was estimated to be 5.7% (52), which is significantly higher than that of D–D fusions. Although not all VH replacements necessarily result in VH genes with long HCDR3s, a high frequency of anti-HIV antibodies contain potential VH replacement footprints and many of these antibodies also have long HCDR3s (52). Seventy-three percent of anti-HIV CD4 induced (CD4i) antibodies and all PGT-class bnAbs (Table 1) contain VH replacement footprints. Both CD4i and PGT antibodies tend to be encoded by IgH genes of long HCDR3s, which are used to reach recessed regions of the Env (39, 52). These observations indicate that VH replacement may contribute significantly to HIV-1 antibodies that use long HCDR3s.

However, the detection of VH replacement by footprint analysis is controversial. Footprint determination of VH replacement could result in false positives because footprints can be mimicked by processes other than VH replacement, such as N-addition (72, 90). It could also result in false negative sequences because not every VH replacement products will have a detectable footprint (85, 90). Yet, footprint analysis is currently the only available choice for VH replacement studies on human primary samples and there is no question that VH replacement can generate antibodies with long HCDR3s.

Discussion

Three of the four potential immunologic mechanisms for the generation of antibodies with long HCDR3s occur mainly at the time of V(D)J recombination during primary B cell development. There are 3.5% B cells with HCDR3s ≥24 amino acid residues and 0.43% B cells with very long HCDR3s (≥28 residues) in the naïve B cell population (68). This is a significant number when one considers the total of more than 1012 potentially different antibodies in the human B cell repertoire. Therefore, long HCDR3s, while relatively low in frequency, are a normal part of the naïve B cell repertoire that can actively participate in humoral immune responses. B cells with long HCDR3s appear to be selected by Env antigens to generate HIV-1 bnAbs targeting conserved epitopes located within deep regions of the HIV-1 envelope trimer. Long HCDR3s alone should not necessarily be viewed as an obstacle to the development of an HIV-1 vaccine targeting the long HCDR3 bnAb responses. Yet, how to induce highly mutated and auto-reactive HIV-1 bnAb response remains a true challenge for HIV-1 vaccine development (60).

The high frequency of VH replacement footprints in many HIV-1 bnAbs suggests a new strategy for HIV-1 vaccine development; we should first understand the mechanism regulating VH replacement events during B cell development (90, 91) and then find a safe procedure to increase the frequency of VH replacement events before immunization. This strategy should increase the frequency of long HCDR3 germline B cells of HIV-1 bnAbs in the naïve B cell pool, which, in turn, may improve the potential of generating bnAb responses against HIV-1. Increasing the frequency of long HCDR3-containing B cells through manipulating the level of VH replacement may lead to more opportunities in generating bnAbs of long CDRH3s. But this remains to be tested because increasing the frequency of HIV-1 bnAbs’ germline B cells may not be sufficient to generate bnAb responses.

Recent studies on the generation of HIV-1 bnAbs in HIV-1 infected individuals have highlighted the co-evolution of the HIV-1 Env diversity and the breadth of neutralizing antibody responses against Env (26, 56, 57, 92), which indicates an antigen-driven pathway for HIV-1 bnAbs. Since it was demonstrated that Envs from different HIV-1 strains are not equal in activating HIV-1 bnAbs’ germline B cells (26, 57, 93), a proper Env antigen with the right conformational epitopes may be required to activate HIV-1 bnAb germline B cells (61, 94) that presumably exist in most healthy individuals. Many of the HIV-1 bnAbs with long HCDR3s, such as PG9 and PGT151, recognize conformational epitopes that are not well exposed in recombinant gp120 or gp140 (30, 46). Therefore, the construction of recombinant Env proteins of native gp140 trimers (39) and/or constrained gp120s (95) that can preferentially expose epitopes recognized by bnAbs would be good antigen candidates in this regard. Further, a proper immunization strategy, such as sequential immunizations with selected diverse Env antigens and proper follicular helper T cells, will likely be required to drive the antibody responses toward highly mutated bnAbs (17, 20, 50).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We would like to thank Dr. George Lewis for helpful conversations, Dr. Marvin Reitz and Dr. Brian Taylor for editing the manuscript. We thank Dr. Anthony West for sharing the Antibody Database [version 2.0(5)]. Yongjun Guan was supported in part by grants 1R56AI098576 and R01AI087181 from NIAID, NIH, and by Grant #OPP1033109 from the Bill and Melinda Gates Foundation.

References

  • 1.Baba TW, Liska V, Hofmann-Lehmann R, Vlasak J, Xu W, Ayehunie S, et al. Human neutralizing monoclonal antibodies of the IgG1 subtype protect against mucosal simian-human immunodeficiency virus infection. Nat Med (2000) 6:200–6 10.1038/72309 [DOI] [PubMed] [Google Scholar]
  • 2.Balazs AB, Ouyang Y, Hong CM, Chen J, Nguyen SM, Rao DS, et al. Vectored immunoprophylaxis protects humanized mice from mucosal HIV transmission. Nat Med (2014) 20:296–300 10.1038/nm.3471 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Barouch DH, Whitney JB, Moldt B, Klein F, Oliveira TY, Liu J, et al. Therapeutic efficacy of potent neutralizing HIV-1-specific monoclonal antibodies in SHIV-infected rhesus monkeys. Nature (2013) 503:224–8 10.1038/nature12744 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Hessell AJ, Poignard P, Hunter M, Hangartner L, Tehrani DM, Bleeker WK, et al. Effective, low-titer antibody protection against low-dose repeated mucosal SHIV challenge in macaques. Nat Med (2009) 15:951–4 10.1038/nm.1974 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Horwitz JA, Halper-Stromberg A, Mouquet H, Gitlin AD, Tretiakova A, Eisenreich TR, et al. HIV-1 suppression and durable control by combining single broadly neutralizing antibodies and antiretroviral drugs in humanized mice. Proc Natl Acad Sci U S A (2013) 110:16538–43 10.1073/pnas.1315295110 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Klein F, Halper-Stromberg A, Horwitz JA, Gruell H, Scheid JF, Bournazos S, et al. HIV therapy by a combination of broadly neutralizing antibodies in humanized mice. Nature (2012) 492:118–22 10.1038/nature11604 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Mascola JR, Lewis MG, Stiegler G, Harris D, VanCott TC, Hayes D, et al. Protection of Macaques against pathogenic simian/human immunodeficiency virus 89.6PD by passive transfer of neutralizing antibodies. J Virol (1999) 73:4009–18 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Moldt B, Rakasz EG, Schultz N, Chan-Hui PY, Swiderek K, Weisgrau KL, et al. Highly potent HIV-specific antibody neutralization in vitro translates into effective protection against mucosal SHIV challenge in vivo. Proc Natl Acad Sci U S A (2012) 109:18921–5 10.1073/pnas.1214785109 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Shibata R, Igarashi T, Haigwood N, Buckler-White A, Ogert R, Ross W, et al. Neutralizing antibody directed against the HIV-1 envelope glycoprotein can completely block HIV-1/SIV chimeric virus infections of macaque monkeys. Nat Med (1999) 5:204–10 10.1038/5568 [DOI] [PubMed] [Google Scholar]
  • 10.Shingai M, Nishimura Y, Klein F, Mouquet H, Donau OK, Plishka R, et al. Antibody-mediated immunotherapy of macaques chronically infected with SHIV suppresses viraemia. Nature (2013) 503:277–80 10.1038/nature12746 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Veazey RS, Shattock RJ, Pope M, Kirijan JC, Jones J, Hu Q, et al. Prevention of virus transmission to macaque monkeys by a vaginally applied monoclonal antibody to HIV-1 gp120. Nat Med (2003) 9:343–6 10.1038/nm833 [DOI] [PubMed] [Google Scholar]
  • 12.Burton DR, Poignard P, Stanfield RL, Wilson IA. Broadly neutralizing antibodies present new prospects to counter highly antigenically diverse viruses. Science (2012) 337:183–6 10.1126/science.1225416 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Haynes BF, McElrath MJ. Progress in HIV-1 vaccine development. Curr Opin HIV AIDS (2013) 8:326–32 10.1097/COH.0b013e328361d178 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Koff WC. HIV vaccine development: challenges and opportunities towards solving the HIV vaccine-neutralizing antibody problem. Vaccine (2011) 30(29):4310–5 10.1016/j.vaccine.2011.11.014 [DOI] [PubMed] [Google Scholar]
  • 15.Kwong PD, Mascola JR, Nabel GJ. The changing face of HIV vaccine research. J Int AIDS Soc (2012) 15:17407. 10.7448/IAS.15.2.17407 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Kwong PD, Mascola JR, Nabel GJ. Broadly neutralizing antibodies and the search for an HIV-1 vaccine: the end of the beginning. Nat Rev Immunol (2013) 13:693–701 10.1038/nri3516 [DOI] [PubMed] [Google Scholar]
  • 17.Mouquet H, Nussenzweig MC. HIV: roadmaps to a vaccine. Nature (2013) 496:441–2 10.1038/nature12091 [DOI] [PubMed] [Google Scholar]
  • 18.Sattentau QJ, McMichael AJ. New templates for HIV-1 antibody-based vaccine design. F1000 Biol Rep (2010) 2:60. 10.3410/B2-60 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Stamatatos L. HIV vaccine design: the neutralizing antibody conundrum. Curr Opin Immunol (2012) 24:316–23 10.1016/j.coi.2012.04.006 [DOI] [PubMed] [Google Scholar]
  • 20.West AP, Jr, Scharf L, Scheid JF, Klein F, Bjorkman PJ, Nussenzweig MC. Structural insights on the role of antibodies in HIV-1 vaccine and therapy. Cell (2014) 156:633–48 10.1016/j.cell.2014.01.052 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Bonsignori M, Hwang KK, Chen X, Tsao CY, Morris L, Gray E, et al. Analysis of a clonal lineage of HIV-1 envelope V2/V3 conformational epitope-specific broadly neutralizing antibodies and their inferred unmutated common ancestors. J Virol (2011) 85:9998–10009 10.1128/JVI.05045-11 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Corti D, Langedijk JP, Hinz A, Seaman MS, Vanzetta F, Fernandez-Rodriguez BM, et al. Analysis of memory B cell responses and isolation of novel monoclonal antibodies with neutralizing breadth from HIV-1-infected individuals. PLoS One (2010) 5:e8805. 10.1371/journal.pone.0008805 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Georgiev IS, Doria-Rose NA, Zhou T, Kwon YD, Staupe RP, Moquin S, et al. Delineating antibody recognition in polyclonal sera from patterns of HIV-1 isolate neutralization. Science (2013) 340:751–6 10.1126/science.1233989 [DOI] [PubMed] [Google Scholar]
  • 24.Huang J, Ofek G, Laub L, Louder MK, Doria-Rose NA, Longo NS, et al. Broad and potent neutralization of HIV-1 by a gp41-specific human antibody. Nature (2012) 491:406–12 10.1038/nature11544 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Li Y, O’Dell S, Wilson R, Wu X, Schmidt SD, Hogerkorp CM, et al. HIV-1 neutralizing antibodies display dual recognition of the primary and coreceptor binding sites and preferential binding to fully cleaved envelope glycoproteins. J Virol (2012) 86:11231–41 10.1128/JVI.01543-12 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Liao HX, Lynch R, Zhou T, Gao F, Alam SM, Boyd SD, et al. Co-evolution of a broadly neutralizing HIV-1 antibody and founder virus. Nature (2013) 496:469–76 10.1038/nature12053 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Scheid JF, Mouquet H, Feldhahn N, Seaman MS, Velinzon K, Pietzsch J, et al. Broad diversity of neutralizing antibodies isolated from memory B cells in HIV-infected individuals. Nature (2009) 458:636–40 10.1038/nature07930 [DOI] [PubMed] [Google Scholar]
  • 28.Scheid JF, Mouquet H, Ueberheide B, Diskin R, Klein F, Oliveira TY, et al. Sequence and structural convergence of broad and potent HIV antibodies that mimic CD4 binding. Science (2011) 333:1633–7 10.1126/science.1207227 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Walker LM, Huber M, Doores KJ, Falkowska E, Pejchal R, Julien JP, et al. Broad neutralization coverage of HIV by multiple highly potent antibodies. Nature (2011) 477:466–70 10.1038/nature10373 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Walker LM, Phogat SK, Chan-Hui PY, Wagner D, Phung P, Goss JL, et al. Broad and potent neutralizing antibodies from an African donor reveal a new HIV-1 vaccine target. Science (2009) 326:285–9 10.1126/science.1178746 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Wu X, Yang ZY, Li Y, Hogerkorp CM, Schief WR, Seaman MS, et al. Rational design of envelope identifies broadly neutralizing human monoclonal antibodies to HIV-1. Science (2010) 329:856–61 10.1126/science.1187659 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Wu X, Zhou T, Zhu J, Zhang B, Georgiev I, Wang C, et al. Focused evolution of HIV-1 neutralizing antibodies revealed by structures and deep sequencing. Science (2011) 333:1593–602 10.1126/science.1207532 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Zhou T, Zhu J, Wu X, Moquin S, Zhang B, Acharya P, et al. Multidonor analysis reveals structural elements, genetic determinants, and maturation pathway for HIV-1 neutralization by VRC01-class antibodies. Immunity (2013) 39:245–58 10.1016/j.immuni.2013.04.012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Chang TW. Selecting low frequency antigen-specific single B lymphocytes. In: Ueberheide B, editor. United States Patent Number 5326696. Houston, TX: Tanox Biosystems, Inc. (1994). [Google Scholar]
  • 35.Scheid JF, Mouquet H, Feldhahn N, Walker BD, Pereyra F, Cutrell E, et al. A method for identification of HIV gp140 binding memory B cells in human blood. J Immunol Methods (2009) 343:65–7 10.1016/j.jim.2008.11.012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Simek MD, Rida W, Priddy FH, Pung P, Carrow E, Laufer DS, et al. Human immunodeficiency virus type 1 elite neutralizers: individuals with broad and potent neutralizing activity identified by using a high-throughput neutralization assay together with an analytical selection algorithm. J Virol (2009) 83:7337–48 10.1128/JVI.00110-09 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Wardemann H, Yurasov S, Schaefer A, Young JW, Meffre E, Nussenzweig MC. Predominant autoantibody production by early human B cell precursors. Science (2003) 301:1374–7 10.1126/science.1086907 [DOI] [PubMed] [Google Scholar]
  • 38.Doores KJ, Fulton Z, Huber M, Wilson IA, Burton DR. Antibody 2G12 recognizes di-mannose equivalently in domain- and nondomain-exchanged forms but only binds the HIV-1 glycan shield if domain exchanged. J Virol (2010) 84:10690–9 10.1128/JVI.01110-10 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Julien JP, Cupo A, Sok D, Stanfield RL, Lyumkis D, Deller MC, et al. Crystal structure of a soluble cleaved HIV-1 envelope trimer. Science (2013) 342:1477–83 10.1126/science.1245625 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Lyumkis D, Julien JP, de Val N, Cupo A, Potter CS, Klasse PJ, et al. Cryo-EM structure of a fully glycosylated soluble cleaved HIV-1 envelope trimer. Science (2013) 342:1484–90 10.1126/science.1245627 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Zhou T, Xu L, Dey B, Hessell AJ, Van Ryk D, Xiang SH, et al. Structural definition of a conserved neutralization epitope on HIV-1 gp120. Nature (2007) 445:732–7 10.1038/nature05580 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Kong L, Lee JH, Doores KJ, Murin CD, Julien JP, McBride R, et al. Supersite of immune vulnerability on the glycosylated face of HIV-1 envelope glycoprotein gp120. Nat Struct Mol Biol (2013) 20(7):796–803 10.1038/nsmb.2594 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Mouquet H, Scharf L, Euler Z, Liu Y, Eden C, Scheid JF, et al. Complex-type N-glycan recognition by potent broadly neutralizing HIV antibodies. Proc Natl Acad Sci U S A (2012) 109:E3268–77 10.1073/pnas.1217207109 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Pejchal R, Doores KJ, Walker LM, Khayat R, Huang PS, Wang SK, et al. A potent and broad neutralizing antibody recognizes and penetrates the HIV glycan shield. Science (2011) 334:1097–103 10.1126/science.1213256 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Blattner C, Lee JH, Sliepen K, Derking R, Falkowska E, de la Pena AT, et al. Structural delineation of a quaternary, cleavage-dependent epitope at the gp41-gp120 interface on intact HIV-1 Env trimers. Immunity (2014) 40:669–80 10.1016/j.immuni.2014.04.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Falkowska E, Le KM, Ramos A, Doores KJ, Lee JH, Blattner C, et al. Broadly neutralizing HIV antibodies define a glycan-dependent epitope on the prefusion conformation of gp41 on cleaved envelope trimers. Immunity (2014) 40:657–68 10.1016/j.immuni.2014.04.009 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Scharf L, Scheid JF, Lee JH, West AP, Jr, Chen C, Gao H, et al. Antibody 8ANC195 reveals a site of broad vulnerability on the HIV-1 envelope spike. Cell Rep (2014) 7(3):785–95 10.1016/j.celrep.2014.04.001 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Buchacher A, Predl R, Strutzenberger K, Steinfellner W, Trkola A, Purtscher M, et al. Generation of human monoclonal antibodies against HIV-1 proteins; electrofusion and Epstein-Barr virus transformation for peripheral blood lymphocyte immortalization. AIDS Res Hum Retroviruses (1994) 10:359–69 10.1089/aid.1994.10.359 [DOI] [PubMed] [Google Scholar]
  • 49.Zhu Z, Qin HR, Chen W, Zhao Q, Shen X, Schutte R, et al. Cross-reactive HIV-1-neutralizing human monoclonal antibodies identified from a patient with 2F5-like antibodies. J Virol (2011) 85:11401–8 10.1128/JVI.05312-11 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Mascola JR, Haynes BF. HIV-1 neutralizing antibodies: understanding nature’s pathways. Immunol Rev (2013) 254:225–44 10.1111/imr.12075 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Lefranc MP, Giudicelli V, Ginestoux C, Jabado-Michaloud J, Folch G, Bellahcene F, et al. IMGT, the international ImMunoGeneTics information system. Nucleic Acids Res (2009) 37:D1006–12 10.1093/nar/gkn838 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Liao H, Guo JT, Lange MD, Fan R, Zemlin M, Su K, et al. Contribution of V(H) replacement products to the generation of anti-HIV antibodies. Clin Immunol (2013) 146:46–55 10.1016/j.clim.2012.11.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Kwong PD, Mascola JR. Human antibodies that neutralize HIV-1: identification, structures, and B cell ontogenies. Immunity (2012) 37:412–25 10.1016/j.immuni.2012.08.012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Tiller T, Tsuiji M, Yurasov S, Velinzon K, Nussenzweig MC, Wardemann H. Autoreactivity in human IgG+ memory B cells. Immunity (2007) 26:205–13 10.1016/j.immuni.2007.01.009 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Wrammert J, Koutsonanos D, Li GM, Edupuganti S, Sui J, Morrissey M, et al. Broadly cross-reactive antibodies dominate the human B cell response against 2009 pandemic H1N1 influenza virus infection. J Exp Med (2011) 208:181–93 10.1084/jem.20101352 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Moore PL, Gray ES, Wibmer CK, Bhiman JN, Nonyane M, Sheward DJ, et al. Evolution of an HIV glycan-dependent broadly neutralizing antibody epitope through immune escape. Nat Med (2012) 18:1688–92 10.1038/nm.2985 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Wibmer CK, Bhiman JN, Gray ES, Tumba N, Abdool Karim SS, Williamson C, et al. Viral escape from HIV-1 neutralizing antibodies drives increased plasma neutralization breadth through sequential recognition of multiple epitopes and immunotypes. PLoS Pathog (2013) 9:e1003738. 10.1371/journal.ppat.1003738 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Victora GD, Nussenzweig MC. Germinal centers. Annu Rev Immunol (2012) 30:429–57 10.1146/annurev-immunol-020711-075032 [DOI] [PubMed] [Google Scholar]
  • 59.Haynes BF, Fleming J, St Clair EW, Katinger H, Stiegler G, Kunert R, et al. Cardiolipin polyspecific autoreactivity in two broadly neutralizing HIV-1 antibodies. Science (2005) 308:1906–8 10.1126/science.1111781 [DOI] [PubMed] [Google Scholar]
  • 60.Verkoczy L, Diaz M. Autoreactivity in HIV-1 broadly neutralizing antibodies: implications for their function and induction by vaccination. Curr Opin HIV AIDS (2014) 9:224–34 10.1097/COH.0000000000000049 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Haynes BF, Kelsoe G, Harrison SC, Kepler TB. B-cell-lineage immunogen design in vaccine development with HIV-1 as a case study. Nat Biotechnol (2012) 30:423–33 10.1038/nbt.2197 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Mouquet H, Nussenzweig MC. Polyreactive antibodies in adaptive immune responses to viruses. Cell Mol Life Sci (2012) 69:1435–45 10.1007/s00018-011-0872-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Ota T, Doyle-Cooper C, Cooper AB, Doores KJ, Aoki-Ota M, Le K, et al. B cells from knock-in mice expressing broadly neutralizing HIV antibody b12 carry an innocuous B cell receptor responsive to HIV vaccine candidates. J Immunol (2013) 191:3179–85 10.4049/jimmunol.1301283 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Wu TT, Johnson G, Kabat EA. Length distribution of CDRH3 in antibodies. Proteins (1993) 16:1–7 10.1002/prot.340160102 [DOI] [PubMed] [Google Scholar]
  • 65.Zemlin M, Klinger M, Link J, Zemlin C, Bauer K, Engler JA, et al. Expressed murine and human CDR-H3 intervals of equal length exhibit distinct repertoires that differ in their amino acid composition and predicted range of structures. J Mol Biol (2003) 334:733–49 10.1016/j.jmb.2003.10.007 [DOI] [PubMed] [Google Scholar]
  • 66.Ivanov II, Schelonka RL, Zhuang Y, Gartland GL, Zemlin M, Schroeder HW., Jr Development of the expressed Ig CDR-H3 repertoire is marked by focusing of constraints in length, amino acid use, and charge that are first established in early B cell progenitors. J Immunol (2005) 174:7773–80 10.4049/jimmunol.174.12.7773 [DOI] [PubMed] [Google Scholar]
  • 67.Arnaout R, Lee W, Cahill P, Honan T, Sparrow T, Weiand M, et al. High-resolution description of antibody heavy-chain repertoires in humans. PLoS One (2011) 6:e22365. 10.1371/journal.pone.0022365 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Briney BS, Willis JR, Crowe JE., Jr Human peripheral blood antibodies with long HCDR3s are established primarily at original recombination using a limited subset of germline genes. PLoS One (2012) 7:e36750. 10.1371/journal.pone.0036750 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Ohno S, Mori N, Matsunaga T. Antigen-binding specificities of antibodies are primarily determined by seven residues of VH. Proc Natl Acad Sci U S A (1985) 82:2945–9 10.1073/pnas.82.9.2945 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Bassing CH, Swat W, Alt FW. The mechanism and regulation of chromosomal V(D)J recombination. Cell (2002) 109(Suppl):S45–55 10.1016/S0092-8674(02)00675-X [DOI] [PubMed] [Google Scholar]
  • 71.Tonegawa S. Somatic generation of antibody diversity. Nature (1983) 302:575–81 10.1038/302575a0 [DOI] [PubMed] [Google Scholar]
  • 72.Briney BS, Crowe JE., Jr Secondary mechanisms of diversification in the human antibody repertoire. Front Immunol (2013) 4:42. 10.3389/fimmu.2013.00042 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Chen C, Nagy Z, Prak EL, Weigert M. Immunoglobulin heavy chain gene replacement: a mechanism of receptor editing. Immunity (1995) 3:747–55 10.1016/1074-7613(95)90064-0 [DOI] [PubMed] [Google Scholar]
  • 74.Wilson PC, Wilson K, Liu YJ, Banchereau J, Pascual V, Capra JD. Receptor revision of immunoglobulin heavy chain variable region genes in normal human B lymphocytes. J Exp Med (2000) 191:1881–94 10.1084/jem.191.11.1881 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Zhang Z, Burrows PD, Cooper MD. The molecular basis and biological significance of VH replacement. Immunol Rev (2004) 197:231–42 10.1111/j.0105-2896.2004.0107.x [DOI] [PubMed] [Google Scholar]
  • 76.Reason DC, Zhou J. Codon insertion and deletion functions as a somatic diversification mechanism in human antibody repertoires. Biol Direct (2006) 1:24. 10.1186/1745-6150-1-24 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Wilson PC, de Bouteiller O, Liu YJ, Potter K, Banchereau J, Capra JD, et al. Somatic hypermutation introduces insertions and deletions into immunoglobulin V genes. J Exp Med (1998) 187:59–70 10.1084/jem.187.1.59 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Briney BS, Willis JR, Crowe JE., Jr Location and length distribution of somatic hypermutation-associated DNA insertions and deletions reveals regions of antibody structural plasticity. Genes Immun (2012) 13:523–9 10.1038/gene.2012.28 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Briney BS, Willis JR, Hicar MD, Thomas JW, II, Crowe JE., Jr Frequency and genetic characterization of V(DD)J recombinants in the human peripheral blood antibody repertoire. Immunology (2012) 137:56–64 10.1111/j.1365-2567.2012.03605.x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Klonowski KD, Primiano LL, Monestier M. Atypical VH-D-JH rearrangements in newborn autoimmune MRL mice. J Immunol (1999) 162:1566–72 [PubMed] [Google Scholar]
  • 81.Sanz I. Multiple mechanisms participate in the generation of diversity of human H chain CDR3 regions. J Immunol (1991) 147:1720–9 [PubMed] [Google Scholar]
  • 82.Watson LC, Moffatt-Blue CS, McDonald RZ, Kompfner E, Ait-Azzouzene D, Nemazee D, et al. Paucity of V-D-D-J rearrangements and VH replacement events in lupus prone and nonautoimmune TdT-/- and TdT+/+ mice. J Immunol (2006) 177:1120–8 10.4049/jimmunol.177.2.1120 [DOI] [PubMed] [Google Scholar]
  • 83.Darlow JM, Stott DI. V(H) replacement in rearranged immunoglobulin genes. Immunology (2005) 114:155–65 10.1111/j.1365-2567.2004.02084.x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Zhang Z, Zemlin M, Wang YH, Munfus D, Huye LE, Findley HW, et al. Contribution of VH gene replacement to the primary B cell repertoire. Immunity (2003) 19:21–31 10.1016/S1074-7613(03)00170-5 [DOI] [PubMed] [Google Scholar]
  • 85.Koralov SB, Novobrantseva TI, Konigsmann J, Ehlich A, Rajewsky K. Antibody repertoires generated by VH replacement and direct VH to JH joining. Immunity (2006) 25:43–53 10.1016/j.immuni.2006.04.016 [DOI] [PubMed] [Google Scholar]
  • 86.Nemazee D. Receptor editing in lymphocyte development and central tolerance. Nat Rev Immunol (2006) 6:728–40 10.1038/nri1939 [DOI] [PubMed] [Google Scholar]
  • 87.Yunk L, Meng W, Cohen PL, Eisenberg RA, Luning Prak ET. Antibodies in a heavy chain knock-in mouse exhibit characteristics of early heavy chain rearrangement. J Immunol (2009) 183:452–61 10.4049/jimmunol.0804060 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 88.Zhang Z. VH replacement in mice and humans. Trends Immunol (2007) 28:132–7 10.1016/j.it.2007.01.003 [DOI] [PubMed] [Google Scholar]
  • 89.Huang L, Lange MD, Zhang Z. VH replacement footprint analyzer-I, a java-based computer program for analyses of immunoglobulin heavy chain genes and potential VH replacement products in human and mouse. Front Immunol (2014) 5:40. 10.3389/fimmu.2014.00040 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Meng W, Jayaraman S, Zhang B, Schwartz GW, Daber RD, Hershberg U, et al. Trials and tribulations with VH replacement. Front Immunol (2014) 5:10. 10.3389/fimmu.2014.00010 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Liu J, Lange MD, Hong SY, Xie W, Xu K, Huang L, et al. Regulation of VH replacement by B cell receptor-mediated signaling in human immature B cells. J Immunol (2013) 190:5559–66 10.4049/jimmunol.1102503 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Doria-Rose NA, Schramm CA, Gorman J, Moore PL, Bhiman JN, DeKosky BJ, et al. Developmental pathway for potent V1V2-directed HIV-neutralizing antibodies. Nature (2014) 509:55–62 10.1038/nature13036 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.McGuire AT, Glenn JA, Lippy A, Stamatatos L. Diverse recombinant HIV-1 Envs fail to activate B cells expressing the germline B cell receptors of the broadly neutralizing anti-HIV-1 antibodies PG9 and 447-52D. J Virol (2014) 88:2645–57 10.1128/JVI.03228-13 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94.Jardine J, Julien JP, Menis S, Ota T, Kalyuzhniy O, McGuire A, et al. Rational HIV immunogen design to target specific germline B cell receptors. Science (2013) 340:711–6 10.1126/science.1234150 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Guan Y, Liu T, Sajadi MM, Yu L, Huang W, Seaman M, et al. A common transitional Env conformation revealed by a new broadly neutralizing antibody as a novel HIV-1 vaccine target. AIDS Vaccine 2013. Barcelona: (2013). 13.56 p. [Google Scholar]

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