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. Author manuscript; available in PMC: 2008 Feb 15.
Published in final edited form as: Mol Immunol. 2005 Sep 2;43(9):1424–1431. doi: 10.1016/j.molimm.2005.07.033

Table 2.

Comparison of the genetic origin of variable regions of anti-MBPS and anti-N-Pr MBPS mAbsa

Clone Isotype VH DH JH VL JK
735 IgG2a,κ IGHV653*01 IGHD-Q52*02 IGHJ2*01 IGKV1-110*02 IGKJ5*01
2-2-B IgM,κ J558.2 IGHD-SP2.7*01 IGHJ2*01 IGKV1-110*01 IGKJ2*01
SEAM 2 IgG3,κ IGHV1S4*01 NDb IGHJ2*01 IGKV1-135*01 IGKJ5*01
SEAM 3 IgG2b,κ IGHV7S3*02 IGHD-SP2.8*01/inv IGHJ2*01 IGKV1-135*01 IGKJ5*01
SEAM 12 IgG2a,κ IGHV13S1*01 IGHD-ST4*01 IGHJ2*01 IGKV4-63*01 IGKJ5*01
SEAM 18 IgG2b,κ IGHV7S3*02 IGHD-SP2.8*01/inv IGHJ2*01 IGKV4-74*01 IGKJ2*01
SEAM 35c IgG2a,κ IGHV7S3*02 NDb IGHJ4*01 IGKV6-20*01 IGKJ2*01
a

Closest matches from either the IGMT or GenBank/EMBL databases. MAb 735 is from a hybridoma produced from a NZB mouse immunized with viable N. meningitidis group B strain ATCC 13090 (Frosch et al., 1985). Since only the amino acid sequences were reported (Klebert et al., 1993; Vaesen et al., 1991), assignment of the germline genes for this mAb was based on the closest match (see Section 2). MAb 2-2-B was produced from a BALB/CJ mouse immunized with N. meningitidis group B strain P355. Germ line assignments were based on the published DNA sequences (Berry et al., 2005). The SEAM mAbs are from hybridomas prepared from CD1 mice immunized with N-Pr MBPS tetanus toxoid conjugate (Granoff et al., 1998).

b

ND, not determined since the segment was too short to enable identification of a specific gene.

c

Note that in our original paper this mAb was listed as being IgG2b, we have subsequently confirmed that it is lgG2a. The subclasses of all of the other anti-N-Pr MBPS mAbs used in this study were retested and confirmed as listed here and in (Granoff et al., 1998).