Stimulation of T cells requires two types of signals - one antigen specific, the other antigen independent. The antigen-independent signal (the costimulatory signal) can be provided by the interaction of B7 molecules with specific receptors on the surface of the T cell. Costimulatory molecules may therefore be useful adjuncts to vaccination. We have cloned and sequenced the rhesus macaque homologues of human B7-1 and B7-2. These molecules are approximately 93-95% homologous to their human counterparts, with amino acid substitutions found throughout the molecule. CHO cells stably expressing B7-1 or B7-2 were recognized by several murine anti-human monoclonal antibodies. To confirm that the rhesus B7 molecules have the same costimulatory function as their human counterparts, CHO cells stably expressing B7-1 or B7-2 were fixed by UV-psoralen treatment and used to stimulate CD4+ T cells that had been suboptimally stimulated with anti-rhesus CD3 monoclonal antibodies. Stimulation of rhesus CD4+ T cells with anti-CD3 mAb alone induced a 5-7 fold increase in T cell proliferation compared with the medium control. Addition of fixed CHO-B7-1 or B7-2 induced a 10-27 fold increase in T cell proliferation compared to anti-CD3 alone. Control vector transfected CHO cells did not induce T cell proliferation over background. T cell proliferation could be blocked by preincubation of CHO B7-1 or B7-2 with anti-human B7-1 or B7-2 antibodies. Rhesus B7-1 and B7-2 molecules were also able to induce human CD4+ T cells to proliferate. The proliferation is specific and can be totally abrogated with anti-human B7-1 or B7-2 monoclonal antibody. After stimulation of rhesus CD4+ T cells, RT-PCR analysis of cytokine production showed that B7-1 stimulated T cells express interleukin 2, 4, 7, 10 and INF-gamma and B7-2 stimulated T cells express interleukin 2, 10 and INF-gamma. These molecular clones of B7-1 and B7-2 will be utilized to enhance in vitro stimulation of cellular immune responses, and to boost immune responses induced by vaccination.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000168-35
Application #
3719011
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
35
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
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