Immune response of SLE patients to peptides based on the complementarity determining regions of a pathogenic anti-dna monoclonal antibody

Molly Dayan, Raphael Segal, Zev Sthoeger, Ari Waisman, Na'ama Brosh, Ori Elkayam, Eran Eilat, Mati Fridkin, Edna Mozes*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

We have examined the humoral and cellular responses of SLE patients to peptides based on the complementarity-determining regions (CDR) of a monoclonal anti-DNA antibody with a major idiotype-16/6 Id, in comparison to their responses to the whole 16/6 Id-bearing antibody. Sera of 63% of the SLE patients had antibodies that bound the 16/6 Id, 80% had antibodies to one of the CDR-based peptides, and 40% of the patients reacted with both CDRs. Sera of only a few controls reacted with either the 16/6 Id (6%) or the CDR based peptides (4%) (P < 0.01). Peripheral blood lymphocytes (PBL) of 39% of the patients proliferated in response to the 16/6 Id or to one of the CDR-based peptides (37%), while in the control group the proliferation rates were 66% to the 16/6 Id and 59% to one of the CDR-based peptides (P < 0.05). The correlation between (both) the humoral and cellular immune responses to the CDR-based peptides and to the 16/6 Id suggests the relevance of these peptides to the 16/6 Id and provides additional information on the pathogenic moiety of the latter antibody.

Original languageEnglish
Pages (from-to)187-194
Number of pages8
JournalJournal of Clinical Immunology
Volume20
Issue number3
DOIs
StatePublished - 2000
Externally publishedYes

Funding

FundersFunder number
Teva Pharmaceutical Industries Limited, Israel

    Keywords

    • Antigen presentation
    • CDR-based peptides
    • SLE
    • T-cell proliferation

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