Literature DB >> 6797934

On evasion of Trypanosoma cruzi from the host immune response. Lymphoproliferative responses to trypanosomal antigens during acute and chronic experimental Chagas' disease.

F Kierszenbaum.   

Abstract

The ability of spleen cells taken from mice infected with Trypanosoma cruzi to proliferate after stimulation with specific trypanosomal antigens was investigated during the acute and chronic phases of the disease. Lymphoproliferation was minimal or undetectable during the acute period whereas the chronic phase was characterized by significant responses over a wide range of antigen concentration. Transfer of infected mouse spleen cells to cultures of splenocytes from chronically infected animals failed to modify the response of the latter to antigenic stimulation as measured by DNA synthesis. Furthermore, the responses of infected mouse spleen cells collected during the acute period and freed of Lyt 2.1-bearing lymphocytes, a subclass known to contain the suppressor T cells, did not differ significantly from those of untreated aliquots of the same cell suspensions. These results, together with the fact that the T-cell compartment of the spleen was severely depleted during the acute but not the chronic stage of the infection, suggest that the impaired immunological responsiveness of acutely infected mice may be due in part to the absence or marked reduction of responder and/or accessory T lymphocytes. An active role for suppressor T cells in the reduced response to trypanosomal antigens by lymphocytes from mice in the early, acute phase of T. cruzi infection is not supported by the present observations.

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Year:  1981        PMID: 6797934      PMCID: PMC1554955     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  22 in total

1.  Suppression of anamnestic cellular responses during experimental American trypanosomiasis.

Authors:  E C Rowland; R E Kuhn
Journal:  J Parasitol       Date:  1978-08       Impact factor: 1.276

2.  Suppression of cellular responses in mice during Trypanosoma cruzi infections.

Authors:  E C Rowland; R E Kuhn
Journal:  Infect Immun       Date:  1978-05       Impact factor: 3.441

3.  Immunobiology of African trypanosomiasis.

Authors:  J M Mansfield
Journal:  Cell Immunol       Date:  1978-08       Impact factor: 4.868

4.  Cytotoxic effects of normal sera on lymphoid cells. III. Selective killing of mouse T cells by normal guinea pig serum.

Authors:  D B Budzko; F Kierszenbaum; B H Waksman
Journal:  J Immunol       Date:  1977-08       Impact factor: 5.422

5.  Suppressor cells in mice infected with Trypanosoma brucei.

Authors:  D D Eardley; A N Jayawardena
Journal:  J Immunol       Date:  1977-09       Impact factor: 5.422

6.  Cellular immunity in chronic Chagas' disease.

Authors:  O M Montufar; C C Musatti; E Mendes; N F Mendes
Journal:  J Clin Microbiol       Date:  1977-04       Impact factor: 5.948

7.  Cytotoxic effects of normal sera on lymphoid cells. I. Antibody-independent killing of heterologous thymocytes by guinea pig, rabbit, and human sera: role of the alternative pathway of complement activation.

Authors:  F Kierszenbaum; D B Budzko
Journal:  Cell Immunol       Date:  1977-03-01       Impact factor: 4.868

8.  Studies of cellular immunity in Chagas disease: effect of glutaraldehyde-treated specific antigen on inhibition of leukocyte migration.

Authors:  R Lelchuk; A Patrucco; J A Manni
Journal:  J Immunol       Date:  1974-04       Impact factor: 5.422

9.  The effects of bacterial endotoxin on the infection of mice with Trypanosoma cruzi.

Authors:  F Kierszenbaum; L E Saavedra
Journal:  J Protozool       Date:  1972-11

10.  Suppression of cell-mediated immunity in experimental Chagas' disease.

Authors:  S G Reed; C L Larson; C A Speer
Journal:  Z Parasitenkd       Date:  1977-06-03
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  15 in total

1.  Humoral and cellular immune responses in BALB/c and C57BL/6 mice immunized with cytoplasmic (CRA) and flagellar (FRA) recombinant repetitive antigens, in acute experimental Trypanosoma cruzi infection.

Authors:  Valéria R A Pereira; Virginia M B Lorena; Mineo Nakazawa; Carlos F Luna; Edimilson D Silva; Antonio G P Ferreira; Marco Aurélio Krieger; Samuel Goldenberg; Milena B P Soares; Eridan M Coutinho; Rodrigo Correa-Oliveira; Yara M Gomes
Journal:  Parasitol Res       Date:  2005-04-27       Impact factor: 2.289

2.  Trypanosoma cruzi-induced suppression of human peripheral blood lymphocytes activated via the alternative (CD2) pathway.

Authors:  L A Beltz; F Kierszenbaum; M B Sztein
Journal:  Infect Immun       Date:  1990-04       Impact factor: 3.441

3.  Selective suppressive effects of Trypanosoma cruzi on activated human lymphocytes.

Authors:  L A Beltz; F Kierszenbaum; M B Sztein
Journal:  Infect Immun       Date:  1989-08       Impact factor: 3.441

4.  Inhibition of Trypanosoma cruzi-specific immune responses by a protein produced by T. cruzi in the course of Chagas' disease.

Authors:  F Kierszenbaum; H M Lopez; M B Sztein
Journal:  Immunology       Date:  1994-03       Impact factor: 7.397

5.  Specific humoral immunity versus polyclonal B cell activation in Trypanosoma cruzi infection of susceptible and resistant mice.

Authors:  Marianne A Bryan; Siobhan E Guyach; Karen A Norris
Journal:  PLoS Negl Trop Dis       Date:  2010-07-06

6.  Effects of extracts of Trypanosoma cruzi on immune responses: induction of a nonspecific suppressor factor.

Authors:  R L Tarleton; R Schafer; R E Kuhn
Journal:  Infect Immun       Date:  1983-09       Impact factor: 3.441

7.  Suppression by Trypanosoma cruzi of T-cell receptor expression by activated human lymphocytes.

Authors:  M B Sztein; F Kierszenbaum
Journal:  Immunology       Date:  1992-10       Impact factor: 7.397

8.  Impairment of monocytic function during Trypanosoma cruzi infection.

Authors:  M J Louie; W R Cuna; C Rodriguez De Cuna; L Mayer; K Sperber
Journal:  Clin Diagn Lab Immunol       Date:  1994-11

9.  Bioluminescent imaging of Trypanosoma cruzi infection.

Authors:  Kenneth V Hyland; Sofya H Asfaw; Cheryl L Olson; Melvin D Daniels; David M Engman
Journal:  Int J Parasitol       Date:  2008-04-25       Impact factor: 3.981

10.  Trypanosoma cruzi-induced immunosuppression: blockade of costimulatory T-cell responses in infected hosts due to defective T-cell receptor-CD3 functioning.

Authors:  M F Lopes; G A dos Reis
Journal:  Infect Immun       Date:  1994-04       Impact factor: 3.441

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