Inactivation of suppressor T cell activity by the nontoxic lipopolysaccharide of Rhodopseudomonas sphaeroides

Author:

Baker P J1,Taylor C E1,Stashak P W1,Fauntleroy M B1,Hasløv K1,Qureshi N1,Takayama K1

Affiliation:

1. Laboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, Rockville, Maryland 20852.

Abstract

Antibody responses of mice immunized with type III pneumococcal polysaccharide were examined with and without treatment with nontoxic lipopolysaccharide from Rhodopseudomonas sphaeroides (Rs-LPS). The results obtained were similar to those described previously for mice treated with monophosphoryl lipid A (MPL) except that lower amounts of Rs-LPS were needed. Both were without effect when given at the time of immunization with type III pneumococcal polysaccharide but elicited significant enhancement when given 2 to 3 days later. Such enhancement was T cell dependent and not due to polyclonal activation of immunoglobulin M synthesis by B cells. Treatment with either Rs-LPS or MPL abolished the expression but not induction of low-dose paralysis, a form of immunological unresponsiveness known to be mediated by suppressor T cells (Ts). The in vitro treatment of cell suspensions containing Ts with extremely small amounts of Rs-LPS or MPI completely eliminated the capacity of such cells to transfer suppression to other mice. These findings indicate that the immunomodulatory effects of both MPL and Rs-LPS are mainly the result of eliminating the inhibitors effects of Ts; this permits the positive effects of amplifier T cells to be more fully expressed, thereby resulting in an increased antibody response. The significance of these and other findings to the use of Rs-LPS as a pharmacotherapeutic agent for gram-negative bacterial sepsis is discussed.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

Reference41 articles.

1. Regulation of the antibody response to type III pneumococcal polysaccharide;Baker P. J.;Rev. Infect. Dis.,1981

2. Direct evidence for the involvement of thymusderived (T) suppressor cells in the expression of low-dose paralysis to type III pneumococcal polysaccharide;Baker P. J.;J. Immunol.,1982

3. Examination of the differential characteristics of amplifier and contrasuppressor T cells;Baker P. J.;Immunobiology,1988

4. Enrichment of suppressor T cells by means of binding to monophosphoryl lipid A;Baker P.;Infect. Immun.,1990

5. Inactivation of suppressor T cell activity by nontoxic monophosphoryl lipid A;Baker P. J.;Infect. Immun.,1988

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