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Comparative analysis of antibody responses against HSP60, invariant surface glycoprotein 70, and variant surface glycoprotein reveals a complex antigen-specific pattern of immunoglobulin isotype switching during infection by Trypanosoma brucei

(2002) INFECTION AND IMMUNITY. 68(2). p.848-860
Author
Organization
Abstract
During Trypanosoma brucei infections, the response against the variant surface glycoprotein (VSG) of the parasite represents a major interaction between the mammalian host immune system and the parasite surface. Since immune recognition of other parasite derived factors also occurs, we examined the humoral host response against trypanosome heat shock protein 60 (HSP60), a conserved antigen with an autoimmune character. During experimental T. brucei infection in BALB/c mice, the anti-HSP60 response was induced when parasites differentiated into stumpy forms. This response was characterized by a stage-specific immunoglobulin isotype switching as well as by the induction of an autoimmune response. Specific recognition of trypanosome HSP60 was found to occur during the entire course of infection. Immunoglobulin G2a (IgG2a) and IgG2b antibodies, induced mainly in a T-cell-independent manner, were observed during the first peak of parasitemia, whereas IgG1 and IgG3 antibodies were found at the end of the infection, due to a specific T-cell-mediated response. Comparative analysis of the kinetics of anti-HSP60, anti-invariant surface glycoprotein 70 (ISG70), and anti-VSG antibody responses indicated that the three trypanosome antigens give rise to specific and independent patterns of immunoglobulin isotype switching.
Keywords
SELF-REACTIVE ANTIBODIES, HEAT-SHOCK PROTEIN-60, AFRICAN TRYPANOSOMES, HEAT-SHOCK-PROTEIN-60 GENE, INTERFERON-GAMMA, CELL RESPONSES, B-CELLS, MICE, EXPRESSION, IMMUNITY

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Chicago
Radwanska, Magdalena, Stefan Magez, A Michel, B Stijlemans, M Geuskens, and E Pays. 2002. “Comparative Analysis of Antibody Responses Against HSP60, Invariant Surface Glycoprotein 70, and Variant Surface Glycoprotein Reveals a Complex Antigen-specific Pattern of Immunoglobulin Isotype Switching During Infection by Trypanosoma Brucei.” Infection and Immunity 68 (2): 848–860.
APA
Radwanska, M., Magez, S., Michel, A., Stijlemans, B., Geuskens, M., & Pays, E. (2002). Comparative analysis of antibody responses against HSP60, invariant surface glycoprotein 70, and variant surface glycoprotein reveals a complex antigen-specific pattern of immunoglobulin isotype switching during infection by Trypanosoma brucei. INFECTION AND IMMUNITY, 68(2), 848–860.
Vancouver
1.
Radwanska M, Magez S, Michel A, Stijlemans B, Geuskens M, Pays E. Comparative analysis of antibody responses against HSP60, invariant surface glycoprotein 70, and variant surface glycoprotein reveals a complex antigen-specific pattern of immunoglobulin isotype switching during infection by Trypanosoma brucei. INFECTION AND IMMUNITY. 2002;68(2):848–60.
MLA
Radwanska, Magdalena et al. “Comparative Analysis of Antibody Responses Against HSP60, Invariant Surface Glycoprotein 70, and Variant Surface Glycoprotein Reveals a Complex Antigen-specific Pattern of Immunoglobulin Isotype Switching During Infection by Trypanosoma Brucei.” INFECTION AND IMMUNITY 68.2 (2002): 848–860. Print.
@article{8528999,
  abstract     = {During Trypanosoma brucei infections, the response against the variant surface glycoprotein (VSG) of the parasite represents a major interaction between the mammalian host immune system and the parasite surface. Since immune recognition of other parasite derived factors also occurs, we examined the humoral host response against trypanosome heat shock protein 60 (HSP60), a conserved antigen with an autoimmune character. During experimental T. brucei infection in BALB/c mice, the anti-HSP60 response was induced when parasites differentiated into stumpy forms. This response was characterized by a stage-specific immunoglobulin isotype switching as well as by the induction of an autoimmune response. Specific recognition of trypanosome HSP60 was found to occur during the entire course of infection. Immunoglobulin G2a (IgG2a) and IgG2b antibodies, induced mainly in a T-cell-independent manner, were observed during the first peak of parasitemia, whereas IgG1 and IgG3 antibodies were found at the end of the infection, due to a specific T-cell-mediated response. Comparative analysis of the kinetics of anti-HSP60, anti-invariant surface glycoprotein 70 (ISG70), and anti-VSG antibody responses indicated that the three trypanosome antigens give rise to specific and independent patterns of immunoglobulin isotype switching.},
  author       = {Radwanska, Magdalena and Magez, Stefan and Michel, A and Stijlemans, B and Geuskens, M and Pays, E},
  issn         = {0019-9567},
  journal      = {INFECTION AND IMMUNITY},
  language     = {eng},
  number       = {2},
  pages        = {848--860},
  title        = {Comparative analysis of antibody responses against HSP60, invariant surface glycoprotein 70, and variant surface glycoprotein reveals a complex antigen-specific pattern of immunoglobulin isotype switching during infection by Trypanosoma brucei},
  url          = {http://dx.doi.org/10.1128/iai.68.2.848-860.2000},
  volume       = {68},
  year         = {2002},
}

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