1. Impaired Antibody Responses but Normal Proliferation of Specific CD4+ T Cells in Mice Lacking Complement Receptors 1 and 2.
- Author
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Carlsson, F., Getahun, A., Rutemark, C., and Heyman, B.
- Subjects
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IMMUNOGLOBULINS , *CELL proliferation , *CD4 antigen , *T cells , *LABORATORY mice - Abstract
Severely impaired Ab responses are seen in animals lacking C (complement) factors C2, C3 or C4 as well as CR1/2 (C receptors 1 and 2). The molecular mechanism behind this phenomenon is not understood. One possibility is that C-containing immune complexes are endocytosed via CR2 on B cells and presented to specific CD4+ T cells, which would then proliferate and provide efficient help to specific B cells. In vitro, B cells can endocytose immune complexes via CR1/2 and present the Ag to T cells. Whether absence of this Ag presenting function in Cr2−/− mice (mice lacking CR1/2) explains their low Ab response is unclear. To address this question, Cr2−/− and wild type mice were transferred with OVA-specific T cells, obtained from the DO11.10 strain which has a transgenic TCR recognizing an OVA peptide. The animals were subsequently immunized with sheep red blood cells (SRBC) conjugated to OVA. Interestingly, proliferation of the OVA-specific T cells was normal in Cr2−/− mice, although their Ab response to both SRBC and OVA was severely impaired. These observations suggest that the impaired Ab response in Cr2−/− mice cannot be explained by a lack of appropriate induction of T cell help. [ABSTRACT FROM AUTHOR]
- Published
- 2009
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