Abstract
The most common organ-specific autoimmune disease in humans involves the thyroid. Autoantibodies against thyroid peroxidase (TPO) are present in the sera of virtually all patients with active disease. We report the molecular cloning of the genes for 30 high-affinity, IgG-class human autoantibodies to TPO from thyroid-infiltrating B cells. Analysis of the putative germline genes used for the TPO human autoantibodies suggests the use of only five different H and L chain combinations involving four H chains and three L chains. In addition, the same combination of H and L chains was found in multiple patients. The F(ab) proteins expressed by these genes define two major, closely associated domains (A and B) in an immunodominant region on TPO. These A and B domains contain the binding sites of approximately 80% of IgG-class TPO autoantibodies in the sera of patients with autoimmune thyroid disease. The present information permits analysis, not previously possible, of the relationship between autoantibody H and L chain genes and the antigenic domains on an autoantigen. Our data, obtained using target organ-derived autoantibodies, indicate that there is restriction in H and L chain usage in relation to the interaction with specific antigenic domains in human, organ-specific autoimmune disease.
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- Beever K., Bradbury J., Phillips D., McLachlan S. M., Pegg C., Goral A., Overbeck W., Feifel G., Smith B. R. Highly sensitive assays of autoantibodies to thyroglobulin and to thyroid peroxidase. Clin Chem. 1989 Sep;35(9):1949–1954. [PubMed] [Google Scholar]
- Berman J. E., Mellis S. J., Pollock R., Smith C. L., Suh H., Heinke B., Kowal C., Surti U., Chess L., Cantor C. R. Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus. EMBO J. 1988 Mar;7(3):727–738. doi: 10.1002/j.1460-2075.1988.tb02869.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burton D. R., Barbas C. F., 3rd Antibodies from libraries. Nature. 1992 Oct 29;359(6398):782–783. doi: 10.1038/359782b0. [DOI] [PubMed] [Google Scholar]
- Casali P., Inghirami G., Nakamura M., Davies T. F., Notkins A. L. Human monoclonals from antigen-specific selection of B lymphocytes and transformation by EBV. Science. 1986 Oct 24;234(4775):476–479. doi: 10.1126/science.3020687. [DOI] [PubMed] [Google Scholar]
- Caton A. J., Koprowski H. Influenza virus hemagglutinin-specific antibodies isolated from a combinatorial expression library are closely related to the immune response of the donor. Proc Natl Acad Sci U S A. 1990 Aug;87(16):6450–6454. doi: 10.1073/pnas.87.16.6450. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen P. P., Liu M. F., Glass C. A., Sinha S., Kipps T. J., Carson D. A. Characterization of two immunoglobulin VH genes that are homologous to human rheumatoid factors. Arthritis Rheum. 1989 Jan;32(1):72–76. doi: 10.1002/anr.1780320112. [DOI] [PubMed] [Google Scholar]
- Davies D. R., Padlan E. A., Sheriff S. Antibody-antigen complexes. Annu Rev Biochem. 1990;59:439–473. doi: 10.1146/annurev.bi.59.070190.002255. [DOI] [PubMed] [Google Scholar]
- Doullay F., Ruf J., Codaccioni J. L., Carayon P. Prevalence of autoantibodies to thyroperoxidase in patients with various thyroid and autoimmune diseases. Autoimmunity. 1991;9(3):237–244. doi: 10.3109/08916939109007649. [DOI] [PubMed] [Google Scholar]
- Eilat D., Fischel R. Recurrent utilization of genetic elements in V regions of antinucleic acid antibodies from autoimmune mice. J Immunol. 1991 Jul 1;147(1):361–368. [PubMed] [Google Scholar]
- Foti D., Kaufman K. D., Chazenbalk G. D., Rapoport B. Generation of a biologically active, secreted form of human thyroid peroxidase by site-directed mutagenesis. Mol Endocrinol. 1990 May;4(5):786–791. doi: 10.1210/mend-4-5-786. [DOI] [PubMed] [Google Scholar]
- Frorath B., Abney C. C., Scanarini M., Berthold H., Hunt N., Northemann W. Mapping of a linear autoantigenic epitope within the human thyroid peroxidase using recombinant DNA techniques. J Biochem. 1992 May;111(5):633–637. doi: 10.1093/oxfordjournals.jbchem.a123810. [DOI] [PubMed] [Google Scholar]
- Fukuma N., Petersen V. B., McLachlan S. M., Pegg C. A., Rees Smith B. Human monoclonal thyroglobulin autoantibodies of high affinity. I. Production, characterisation and interaction with murine monoclonal thyroglobulin antibodies. Autoimmunity. 1991;10(4):291–295. doi: 10.3109/08916939109001903. [DOI] [PubMed] [Google Scholar]
- Gardas A., Domek H. The effect of sulphydryl reagents on the human thyroid microsomal antigen. J Endocrinol Invest. 1988 May;11(5):385–388. doi: 10.1007/BF03349061. [DOI] [PubMed] [Google Scholar]
- Gherardi E., Milstein C. Original and artificial antibodies. Nature. 1992 May 21;357(6375):201–202. doi: 10.1038/357201a0. [DOI] [PubMed] [Google Scholar]
- Gleason S. L., Gearhart P., Rose N. R., Kuppers R. C. Autoantibodies to thyroglobulin are encoded by diverse V-gene segments and recognize restricted epitopes. J Immunol. 1990 Sep 15;145(6):1768–1775. [PubMed] [Google Scholar]
- Han J. H., Stratowa C., Rutter W. J. Isolation of full-length putative rat lysophospholipase cDNA using improved methods for mRNA isolation and cDNA cloning. Biochemistry. 1987 Mar 24;26(6):1617–1625. doi: 10.1021/bi00380a020. [DOI] [PubMed] [Google Scholar]
- Hexham J. M., Persson M. A., Pegg C., Burton D. R., Furmaniak J., Rees Smith B. Cloning and expression of a human thyroglobulin autoantibody. Autoimmunity. 1991;11(1):69–70. doi: 10.3109/08916939108994711. [DOI] [PubMed] [Google Scholar]
- Laing P. Antigen binding characteristics of thyroid microsomal autoantibodies studied with ELISA methods. J Clin Lab Immunol. 1986 Jan;19(1):19–23. [PubMed] [Google Scholar]
- Lucas A. H., Granoff D. M. A major crossreactive idiotype associated with human antibodies to the Haemophilus influenzae b polysaccharide. Expression in relation to age and immunoglobulin G subclass. J Clin Invest. 1990 Apr;85(4):1158–1166. doi: 10.1172/JCI114548. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Magnusson R. P., Chazenbalk G. D., Gestautas J., Seto P., Filetti S., DeGroot L. J., Rapoport B. Molecular cloning of the complementary deoxyribonucleic acid for human thyroid peroxidase. Mol Endocrinol. 1987 Nov;1(11):856–861. doi: 10.1210/mend-1-11-856. [DOI] [PubMed] [Google Scholar]
- Manheimer-Lory A., Katz J. B., Pillinger M., Ghossein C., Smith A., Diamond B. Molecular characteristics of antibodies bearing an anti-DNA-associated idiotype. J Exp Med. 1991 Dec 1;174(6):1639–1652. doi: 10.1084/jem.174.6.1639. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marks J. D., Tristem M., Karpas A., Winter G. Oligonucleotide primers for polymerase chain reaction amplification of human immunoglobulin variable genes and design of family-specific oligonucleotide probes. Eur J Immunol. 1991 Apr;21(4):985–991. doi: 10.1002/eji.1830210419. [DOI] [PubMed] [Google Scholar]
- Martin A., Davies T. F. T cells and human autoimmune thyroid disease: emerging data show lack of need to invoke suppressor T cell problems. Thyroid. 1992 Fall;2(3):247–261. doi: 10.1089/thy.1992.2.247. [DOI] [PubMed] [Google Scholar]
- McLachlan S. M., Rapoport B. The molecular biology of thyroid peroxidase: cloning, expression and role as autoantigen in autoimmune thyroid disease. Endocr Rev. 1992 May;13(2):192–206. doi: 10.1210/edrv-13-2-192. [DOI] [PubMed] [Google Scholar]
- Mullinax R. L., Gross E. A., Amberg J. R., Hay B. N., Hogrefe H. H., Kubitz M. M., Greener A., Alting-Mees M., Ardourel D., Short J. M. Identification of human antibody fragment clones specific for tetanus toxoid in a bacteriophage lambda immunoexpression library. Proc Natl Acad Sci U S A. 1990 Oct;87(20):8095–8099. doi: 10.1073/pnas.87.20.8095. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nagayama Y., Rapoport B. The thyrotropin receptor 25 years after its discovery: new insight after its molecular cloning. Mol Endocrinol. 1992 Feb;6(2):145–156. doi: 10.1210/mend.6.2.1569961. [DOI] [PubMed] [Google Scholar]
- Nakajima Y., Howells R. D., Pegg C., Jones E. D., Smith B. R. Structure-activity analysis of microsomal antigen/thyroid peroxidase. Mol Cell Endocrinol. 1987 Sep;53(1-2):15–23. doi: 10.1016/0303-7207(87)90187-0. [DOI] [PubMed] [Google Scholar]
- Nye L., Pontes de Carvalho L. C., Roitt I. M. Restrictions in the response to autologous thyroglobulin in the human. Clin Exp Immunol. 1980 Aug;41(2):252–263. [PMC free article] [PubMed] [Google Scholar]
- O'Keefe T. L., Bandyopadhyay S., Datta S. K., Imanishi-Kari T. V region sequences of an idiotypically connected family of pathogenic anti-DNA autoantibodies. J Immunol. 1990 Jun 1;144(11):4275–4283. [PubMed] [Google Scholar]
- Olee T., Lu E. W., Huang D. F., Soto-Gil R. W., Deftos M., Kozin F., Carson D. A., Chen P. P. Genetic analysis of self-associating immunoglobulin G rheumatoid factors from two rheumatoid synovia implicates an antigen-driven response. J Exp Med. 1992 Mar 1;175(3):831–842. doi: 10.1084/jem.175.3.831. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Olee T., Yang P. M., Siminovitch K. A., Olsen N. J., Hillson J., Wu J., Kozin F., Carson D. A., Chen P. P. Molecular basis of an autoantibody-associated restriction fragment length polymorphism that confers susceptibility to autoimmune diseases. J Clin Invest. 1991 Jul;88(1):193–203. doi: 10.1172/JCI115277. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Panosian-Sahakian N., Klotz J. L., Ebling F., Kronenberg M., Hahn B. Diversity of Ig V gene segments found in anti-DNA autoantibodies from a single (NZB x NZW)F1 mouse. J Immunol. 1989 Jun 15;142(12):4500–4506. [PubMed] [Google Scholar]
- Pargent W., Meindl A., Thiebe R., Mitzel S., Zachau H. G. The human immunoglobulin kappa locus. Characterization of the duplicated O regions. Eur J Immunol. 1991 Aug;21(8):1821–1827. doi: 10.1002/eji.1830210807. [DOI] [PubMed] [Google Scholar]
- Parkes A. B., McLachlan S. M., Bird P., Rees Smith B. The distribution of microsomal and thyroglobulin antibody activity among the IgG subclasses. Clin Exp Immunol. 1984 Jul;57(1):239–243. [PMC free article] [PubMed] [Google Scholar]
- Pascual V., Capra J. D. Human immunoglobulin heavy-chain variable region genes: organization, polymorphism, and expression. Adv Immunol. 1991;49:1–74. doi: 10.1016/s0065-2776(08)60774-9. [DOI] [PubMed] [Google Scholar]
- Pascual V., Capra J. D. VH4-21, a human VH gene segment overrepresented in the autoimmune repertoire. Arthritis Rheum. 1992 Jan;35(1):11–18. doi: 10.1002/art.1780350103. [DOI] [PubMed] [Google Scholar]
- Pascual V., Victor K., Randen I., Thompson K., Steinitz M., Førre O., Fu S. M., Natvig J. B., Capra J. D. Nucleotide sequence analysis of rheumatoid factors and polyreactive antibodies derived from patients with rheumatoid arthritis reveals diverse use of VH and VL gene segments and extensive variability in CDR-3. Scand J Immunol. 1992 Aug;36(2):349–362. doi: 10.1111/j.1365-3083.1992.tb03108.x. [DOI] [PubMed] [Google Scholar]
- Persson M. A., Caothien R. H., Burton D. R. Generation of diverse high-affinity human monoclonal antibodies by repertoire cloning. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2432–2436. doi: 10.1073/pnas.88.6.2432. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Phillips D., McLachlan S., Stephenson A., Roberts D., Moffitt S., McDonald D., Ad'Hiah A., Stratton A., Young E., Clark F. Autosomal dominant transmission of autoantibodies to thyroglobulin and thyroid peroxidase. J Clin Endocrinol Metab. 1990 Mar;70(3):742–746. doi: 10.1210/jcem-70-3-742. [DOI] [PubMed] [Google Scholar]
- Phillips D., Prentice L., Upadhyaya M., Lunt P., Chamberlain S., Roberts D. F., McLachlan S., Smith B. R. Autosomal dominant inheritance of autoantibodies to thyroid peroxidase and thyroglobulin--studies in families not selected for autoimmune thyroid disease. J Clin Endocrinol Metab. 1991 May;72(5):973–975. doi: 10.1210/jcem-72-5-973. [DOI] [PubMed] [Google Scholar]
- Portolano S., Chazenbalk G. D., Hutchison J. S., McLachlan S. M., Rapoport B. Lack of promiscuity in autoantigen-specific H and L chain combinations as revealed by human H and L chain "roulette". J Immunol. 1993 Feb 1;150(3):880–887. [PubMed] [Google Scholar]
- Portolano S., Chazenbalk G. D., Seto P., Hutchison J. S., Rapoport B., McLachlan S. M. Recognition by recombinant autoimmune thyroid disease-derived Fab fragments of a dominant conformational epitope on human thyroid peroxidase. J Clin Invest. 1992 Sep;90(3):720–726. doi: 10.1172/JCI115943. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Portolano S., Seto P., Chazenbalk G. D., Nagayama Y., McLachlan S. M., Rapoport B. A human Fab fragment specific for thyroid peroxidase generated by cloning thyroid lymphocyte-derived immunoglobulin genes in a bacteriophage lambda library. Biochem Biophys Res Commun. 1991 Aug 30;179(1):372–377. doi: 10.1016/0006-291x(91)91380-u. [DOI] [PubMed] [Google Scholar]
- Prentice L. M., Phillips D. I., Sarsero D., Beever K., McLachlan S. M., Smith B. R. Geographical distribution of subclinical autoimmune thyroid disease in Britain: a study using highly sensitive direct assays for autoantibodies to thyroglobulin and thyroid peroxidase. Acta Endocrinol (Copenh) 1990 Nov;123(5):493–498. doi: 10.1530/acta.0.1230493. [DOI] [PubMed] [Google Scholar]
- Randen I., Brown D., Thompson K. M., Hughes-Jones N., Pascual V., Victor K., Capra J. D., Førre O., Natvig J. B. Clonally related IgM rheumatoid factors undergo affinity maturation in the rheumatoid synovial tissue. J Immunol. 1992 May 15;148(10):3296–3301. [PubMed] [Google Scholar]
- Rees Smith B., McLachlan S. M., Furmaniak J. Autoantibodies to the thyrotropin receptor. Endocr Rev. 1988 Feb;9(1):106–121. doi: 10.1210/edrv-9-1-106. [DOI] [PubMed] [Google Scholar]
- Ruf J., Toubert M. E., Czarnocka B., Durand-Gorde J. M., Ferrand M., Carayon P. Relationship between immunological structure and biochemical properties of human thyroid peroxidase. Endocrinology. 1989 Sep;125(3):1211–1218. doi: 10.1210/endo-125-3-1211. [DOI] [PubMed] [Google Scholar]
- Salacinski P. R., McLean C., Sykes J. E., Clement-Jones V. V., Lowry P. J. Iodination of proteins, glycoproteins, and peptides using a solid-phase oxidizing agent, 1,3,4,6-tetrachloro-3 alpha,6 alpha-diphenyl glycoluril (Iodogen). Anal Biochem. 1981 Oct;117(1):136–146. doi: 10.1016/0003-2697(81)90703-x. [DOI] [PubMed] [Google Scholar]
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanz I., Casali P., Thomas J. W., Notkins A. L., Capra J. D. Nucleotide sequences of eight human natural autoantibody VH regions reveals apparent restricted use of VH families. J Immunol. 1989 Jun 1;142(11):4054–4061. [PubMed] [Google Scholar]
- Schardt C. W., McLachlan S. M., Matheson J., Smith B. R. An enzyme-linked immunoassay for thyroid microsomal antibodies. J Immunol Methods. 1982 Dec 17;55(2):155–168. doi: 10.1016/0022-1759(82)90028-x. [DOI] [PubMed] [Google Scholar]
- Shin E. K., Matsuda F., Nagaoka H., Fukita Y., Imai T., Yokoyama K., Soeda E., Honjo T. Physical map of the 3' region of the human immunoglobulin heavy chain locus: clustering of autoantibody-related variable segments in one haplotype. EMBO J. 1991 Dec;10(12):3641–3645. doi: 10.1002/j.1460-2075.1991.tb04930.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shlomchik M. J., Marshak-Rothstein A., Wolfowicz C. B., Rothstein T. L., Weigert M. G. The role of clonal selection and somatic mutation in autoimmunity. 1987 Aug 27-Sep 2Nature. 328(6133):805–811. doi: 10.1038/328805a0. [DOI] [PubMed] [Google Scholar]
- Takahashi N., Ueda S., Obata M., Nikaido T., Nakai S., Honjo T. Structure of human immunoglobulin gamma genes: implications for evolution of a gene family. Cell. 1982 Jun;29(2):671–679. doi: 10.1016/0092-8674(82)90183-0. [DOI] [PubMed] [Google Scholar]
- Tomlinson I. M., Walter G., Marks J. D., Llewelyn M. B., Winter G. The repertoire of human germline VH sequences reveals about fifty groups of VH segments with different hypervariable loops. J Mol Biol. 1992 Oct 5;227(3):776–798. doi: 10.1016/0022-2836(92)90223-7. [DOI] [PubMed] [Google Scholar]
- Victor K. D., Pascual V., Lefvert A. K., Capra J. D. Human anti-acetylcholine receptor antibodies use variable gene segments analogous to those used in autoantibodies of various specificities. Mol Immunol. 1992 Dec;29(12):1501–1506. doi: 10.1016/0161-5890(92)90224-l. [DOI] [PubMed] [Google Scholar]
- Weetman A. P., Black C. M., Cohen S. B., Tomlinson R., Banga J. P., Reimer C. B. Affinity purification of IgG subclasses and the distribution of thyroid auto-antibody reactivity in Hashimoto's thyroiditis. Scand J Immunol. 1989 Jul;30(1):73–82. doi: 10.1111/j.1365-3083.1989.tb01190.x. [DOI] [PubMed] [Google Scholar]
- Weisbart R. H., Wong A. L., Noritake D., Kacena A., Chan G., Ruland C., Chin E., Chen I. S., Rosenblatt J. D. The rheumatoid factor reactivity of a human IgG monoclonal autoantibody is encoded by a variant V kappa II L chain gene. J Immunol. 1991 Oct 15;147(8):2795–2801. [PubMed] [Google Scholar]
- Yoshida H., Amino N., Yagawa K., Uemura K., Satoh M., Miyai K., Kumahara Y. Association of serum antithyroid antibodies with lymphocytic infiltration of the thyroid gland: studies of seventy autopsied cases. J Clin Endocrinol Metab. 1978 Jun;46(6):859–862. doi: 10.1210/jcem-46-6-859. [DOI] [PubMed] [Google Scholar]
- van Es J. H., Gmelig Meyling F. H., van de Akker W. R., Aanstoot H., Derksen R. H., Logtenberg T. Somatic mutations in the variable regions of a human IgG anti-double-stranded DNA autoantibody suggest a role for antigen in the induction of systemic lupus erythematosus. J Exp Med. 1991 Feb 1;173(2):461–470. doi: 10.1084/jem.173.2.461. [DOI] [PMC free article] [PubMed] [Google Scholar]


