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Research Article Free access | 10.1172/JCI113483

Complete protein sequences of the variable regions of the cloned heavy and light chains of a human anti-cytomegalovirus antibody reveal a striking similarity to human monoclonal rheumatoid factors of the Wa idiotypic family.

M M Newkirk, H Gram, G F Heinrich, L Ostberg, J D Capra, and R L Wasserman

Department of Microbiology, University of Texas Health Sciences Center, Dallas 75235.

Find articles by Newkirk, M. in: PubMed | Google Scholar

Department of Microbiology, University of Texas Health Sciences Center, Dallas 75235.

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Department of Microbiology, University of Texas Health Sciences Center, Dallas 75235.

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Department of Microbiology, University of Texas Health Sciences Center, Dallas 75235.

Find articles by Ostberg, L. in: PubMed | Google Scholar

Department of Microbiology, University of Texas Health Sciences Center, Dallas 75235.

Find articles by Capra, J. in: PubMed | Google Scholar

Department of Microbiology, University of Texas Health Sciences Center, Dallas 75235.

Find articles by Wasserman, R. in: PubMed | Google Scholar

Published May 1, 1988 - More info

Published in Volume 81, Issue 5 on May 1, 1988
J Clin Invest. 1988;81(5):1511–1518. https://doi.org/10.1172/JCI113483.
© 1988 The American Society for Clinical Investigation
Published May 1, 1988 - Version history
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Abstract

The complete amino acid and nucleotide sequences of the variable regions of the heavy and light polypeptide chains of a human neutralizing IgGl anti-cytomegalovirus (CMV) antibody reveal a striking homology to IgM rheumatoid factors (RFs) of the Wa idiotypic family. The anti-CMV antibody and Wa RFs have in common VKIIIb, JKl, and VHIa gene segments but use different DH and JH gene segments. The anti-CMV antibody does not have RF activity and does not express the Wa idiotype. The Wa RFs do not have anti-CMV activity. A subset of Wa RFs, however, and the anti-CMV antibody do share several idiotypes on the VHIa and VKIIIb polypeptides. Since there are major differences in the antigen binding characteristics and some of the other expressed idiotypes, these data suggest that the D and J region amino acids are crucial to such specificities. Although the use of such highly homologous gene segments in different immune responses is well-documented in murine systems, these data represent the first such example in the human.

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