T/B-cell interactions are more transient in response to weak stimuli in SLE-prone mice

Parisa Sinai, Igor M Dozmorov, Ran Song, Pamela L Schwartzberg, Edward K Wakeland, Christoph Wülfing, Christoph Wülfing

Research output: Contribution to journalArticle (Academic Journal)peer-review

17 Citations (Scopus)


Changes in immune function during the course of systemic lupus erythematosus (SLE) are well characterized. Class-switched antinuclear antibodies are the hallmark of SLE, and T/B-cell interactions are thus critical. However, changes in immune function contributing to disease susceptibility are unknown. Here, we have analyzed primary T and B cells from a mouse model of SLE prior to the onset of disease. To allow cognate T-cell activation with low affinity, we have developed a lower potency peptide ligand for the OTII TCR. T- and B-cell couples formed less frequently and retained their polarity less efficiently preferentially in response to low-affinity stimulation in SLE-prone mice. This matched decreased recruitment of actin and Vav1 and an enhanced PKCΘ recruitment to the cellular interface in T cells. The induction of the GC B-cell marker GL7 was increased in T/B cell couples from SLE-prone mice when the T-cell numbers were limited. However, the overall gene expression changes were marginal. Taken together, the enhanced cell-couple transience may allow a more efficient sampling of a large number of T/B cell couples, preferentially in response to limiting stimuli, therefore enhancing the immune reactivity in the development of SLE.

Original languageEnglish
Pages (from-to)3522-31
Number of pages10
JournalEuropean Journal of Immunology
Issue number12
Publication statusPublished - Dec 2014

Bibliographical note

© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.


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