Affiliation:
1. Department of Immunology, The Weizmann Institute of Science,1 and
2. ProSpec-TechnoGene, Weizmann Science Park,2 Rehovot, Israel, and
3. Immunobiological Research Institute Siena (IRIS), 53100 Siena, Italy3
Abstract
ABSTRACT
Pertussis toxin (PT), a holomer consisting of a catalytic S1 subunit and a B oligomer composed of S2-S4 and S3-S4 dimers, held together by the S5 subunit, exerts profound effects on immune cells, including T-cell mitogenicity. While the mitogenic activity of PT was shown to reside fully within the B oligomer, it could not be assigned to any particular B-oligomer component. In this study, we purified the S3-S4 dimer to homogeneity under conditions propitious to maintenance of the native conformation. In contrast to previous reports which suggested that both S3-S4 and S2-S4 dimers are necessary for mitogenic activity, our preparation of the highly purified S3-S4 dimer was as strongly mitogenic as the B oligomer, suggesting that the S3-S4 dimer accounts for the mitogenic activity of the B oligomer. Moreover, in vitro stimulation of naive lymphocytes by the S3-S4 dimer resulted in reversal of the normal CD4
+
/CD8
+
T-cell ratio from approximately 2:1 to 1:2. The reversal of the CD4
+
/CD8
+
T-cell ratio is unlikely to be due to preferential apoptosis-necrosis of CD4
+
T cells, as indicated by fluorescence-activated cell sorter analysis of annexin-stained T-cell subsets, or to preferential stimulation of CD8
+
T cells. The mechanism underlying the reversal requires further investigation. Nevertheless, the data presented indicate that the S3-S4 dimer may have potential use in the context of diseases amenable to immunological modulation.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Reference37 articles.
1. Pertussis holotoxoid formed in vitro with a genetically deactivated S1 subunit;Bartley T. D.;Proc. Natl. Acad. Sci. USA,1989
2. Detection of cells responding to myelin basic protein by proliferation and selection of T cell lines functional in mediating experimental autoimmune encephalomyelitis in mice;Ben-Nun A.;J. Immunol.,1983
3. Immunomodulation of murine experimental autoimmune encephalomyelitis by pertussis toxin: the protective activity, but not the disease-enhancing activity, can be attributed to the nontoxic B-oligomer;Ben-Nun A.;Proc. Assoc. Am. Phys.,1997
4. Protection against autoimmune disease by bacterial agents. II. PPD and pertussis toxin as proteins active in protecting mice against experimental autoimmune encephalomyelitis;Ben-Nun A.;Eur. J. Immunol.,1993
5. ADP-ribosyltransferase activity of pertussis toxin and immunomodulation by Bordetella pertussis;Black W. J.;Science,1988
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