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A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis

BACKGROUND: Collagen XI (CXI) is a heterotrimeric molecule with triple helical structure in which the α3(XI) chain is identical to the α1(II) chain of collagen II (CII), but with extensive posttranslational modifications. CXI molecules are intermingled in the cartilage collagen fibers, which are mai...

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Autores principales: Tong, Dongmei, Lönnblom, Erik, Yau, Anthony C. Y., Nandakumar, Kutty Selva, Liang, Bibo, Ge, Changrong, Viljanen, Johan, Li, Lei, Bãlan, Mirela, Klareskog, Lars, Chagin, Andrei S., Gjertsson, Inger, Kihlberg, Jan, Zhao, Ming, Holmdahl, Rikard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906551/
https://www.ncbi.nlm.nih.gov/pubmed/29706949
http://dx.doi.org/10.3389/fimmu.2018.00451
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author Tong, Dongmei
Lönnblom, Erik
Yau, Anthony C. Y.
Nandakumar, Kutty Selva
Liang, Bibo
Ge, Changrong
Viljanen, Johan
Li, Lei
Bãlan, Mirela
Klareskog, Lars
Chagin, Andrei S.
Gjertsson, Inger
Kihlberg, Jan
Zhao, Ming
Holmdahl, Rikard
author_facet Tong, Dongmei
Lönnblom, Erik
Yau, Anthony C. Y.
Nandakumar, Kutty Selva
Liang, Bibo
Ge, Changrong
Viljanen, Johan
Li, Lei
Bãlan, Mirela
Klareskog, Lars
Chagin, Andrei S.
Gjertsson, Inger
Kihlberg, Jan
Zhao, Ming
Holmdahl, Rikard
author_sort Tong, Dongmei
collection PubMed
description BACKGROUND: Collagen XI (CXI) is a heterotrimeric molecule with triple helical structure in which the α3(XI) chain is identical to the α1(II) chain of collagen II (CII), but with extensive posttranslational modifications. CXI molecules are intermingled in the cartilage collagen fibers, which are mainly composed of CII. One of the alpha chains in CXI is shared with CII and contains the immunodominant T cell epitope, but it is unclear whether there are shared B cell epitopes as the antibodies tend to recognize the triple helical structures. METHODS: Mice expressing the susceptible immune response gene Aq were immunized with CII or CXI. Serum antibody responses were measured, monoclonal antibodies were isolated and analyzed for specificity to CII, CXI, and triple helical collagen peptides using bead-based multiplex immunoassays, enzyme-linked immunosorbent assays, and Western blots. Arthritogenicity of the antibodies was investigated by passive transfer experiments. RESULTS: Immunization with CII or CXI leads to a strong T and B cell response, including a cross-reactive response to both collagen types. Immunization with CII leads to severe arthritis in mice, with a response toward CXI at the chronic stage, whereas CXI immunization induces very mild arthritis only. A series of monoclonal antibodies to CXI were isolated and of these, the L10D9 antibody bound to both CXI and CII equally strong, with a specific binding for the D3 epitope region of α3(XI) or α1(II) chain. The L10D9 antibody binds cartilage in vivo and induced severe arthritis. In contrast, the L5F3 antibody only showed weak binding and L7D8 antibody has no binding to cartilage and did not induce arthritis. The arthritogenic L10D9 antibody bound to an epitope shared with CII, the triple helical D3 epitope. Antibody levels to the shared D3 epitope were elevated in the sera from mice with arthritis as well as in rheumatoid arthritis. CONCLUSION: CXI is immunologically not exposed in healthy cartilage but contains T and B cell epitopes cross-reactive with CII, which could be activated in both mouse and human arthritis and could evoke an arthritogenic response.
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spelling pubmed-59065512018-04-27 A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis Tong, Dongmei Lönnblom, Erik Yau, Anthony C. Y. Nandakumar, Kutty Selva Liang, Bibo Ge, Changrong Viljanen, Johan Li, Lei Bãlan, Mirela Klareskog, Lars Chagin, Andrei S. Gjertsson, Inger Kihlberg, Jan Zhao, Ming Holmdahl, Rikard Front Immunol Immunology BACKGROUND: Collagen XI (CXI) is a heterotrimeric molecule with triple helical structure in which the α3(XI) chain is identical to the α1(II) chain of collagen II (CII), but with extensive posttranslational modifications. CXI molecules are intermingled in the cartilage collagen fibers, which are mainly composed of CII. One of the alpha chains in CXI is shared with CII and contains the immunodominant T cell epitope, but it is unclear whether there are shared B cell epitopes as the antibodies tend to recognize the triple helical structures. METHODS: Mice expressing the susceptible immune response gene Aq were immunized with CII or CXI. Serum antibody responses were measured, monoclonal antibodies were isolated and analyzed for specificity to CII, CXI, and triple helical collagen peptides using bead-based multiplex immunoassays, enzyme-linked immunosorbent assays, and Western blots. Arthritogenicity of the antibodies was investigated by passive transfer experiments. RESULTS: Immunization with CII or CXI leads to a strong T and B cell response, including a cross-reactive response to both collagen types. Immunization with CII leads to severe arthritis in mice, with a response toward CXI at the chronic stage, whereas CXI immunization induces very mild arthritis only. A series of monoclonal antibodies to CXI were isolated and of these, the L10D9 antibody bound to both CXI and CII equally strong, with a specific binding for the D3 epitope region of α3(XI) or α1(II) chain. The L10D9 antibody binds cartilage in vivo and induced severe arthritis. In contrast, the L5F3 antibody only showed weak binding and L7D8 antibody has no binding to cartilage and did not induce arthritis. The arthritogenic L10D9 antibody bound to an epitope shared with CII, the triple helical D3 epitope. Antibody levels to the shared D3 epitope were elevated in the sera from mice with arthritis as well as in rheumatoid arthritis. CONCLUSION: CXI is immunologically not exposed in healthy cartilage but contains T and B cell epitopes cross-reactive with CII, which could be activated in both mouse and human arthritis and could evoke an arthritogenic response. Frontiers Media S.A. 2018-04-12 /pmc/articles/PMC5906551/ /pubmed/29706949 http://dx.doi.org/10.3389/fimmu.2018.00451 Text en Copyright © 2018 Tong, Lönnblom, Yau, Nandakumar, Liang, Ge, Viljanen, Li, Bãlan, Klareskog, Chagin, Gjertsson, Kihlberg, Zhao and Holmdahl. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Tong, Dongmei
Lönnblom, Erik
Yau, Anthony C. Y.
Nandakumar, Kutty Selva
Liang, Bibo
Ge, Changrong
Viljanen, Johan
Li, Lei
Bãlan, Mirela
Klareskog, Lars
Chagin, Andrei S.
Gjertsson, Inger
Kihlberg, Jan
Zhao, Ming
Holmdahl, Rikard
A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis
title A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis
title_full A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis
title_fullStr A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis
title_full_unstemmed A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis
title_short A Shared Epitope of Collagen Type XI and Type II Is Recognized by Pathogenic Antibodies in Mice and Humans with Arthritis
title_sort shared epitope of collagen type xi and type ii is recognized by pathogenic antibodies in mice and humans with arthritis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906551/
https://www.ncbi.nlm.nih.gov/pubmed/29706949
http://dx.doi.org/10.3389/fimmu.2018.00451
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