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Passive Administration of Monoclonal Antibodies Against H. capsulatum and Others Fungal Pathogens
Published on: February 15, 2011
Functional analysis of Histoplasma capsulatum-reactive T-cell hybridomas
1Department of Internal Medicine, University of Cincinnati College of Medicine, Ohio 45267-0560.
Insights
Researchers developed CD4+ T-cell hybridomas to study Histoplasma capsulatum immune responses. These hybridomas effectively identified key yeast-phase antigens, aiding in understanding T-cell activation against fungal infections.
Area of Science:
- Immunology
- Mycology
- Cell Biology
Background:
- CD4+ T-cell activation is vital for clearing Histoplasma capsulatum infections.
- Limited data exists on the immunobiology of CD4+ T cells reactive to H. capsulatum.
Purpose of the Study:
- To create murine T-cell hybridomas for analyzing CD4+ T-cell functions against H. capsulatum.
- To identify specific yeast-phase antigens recognized by these T cells.
Main Methods:
- Developed 10 CD4+ murine T-cell hybridomas from immune C57BL/6 mice splenocytes.
- Stimulated hybridomas with histoplasmin and yeast-phase preparations (cytosol, cell wall, cell membrane).
- Utilized one-dimensional T-cell immunoblotting to map antigenic determinants.
Main Results:
- Hybridomas released interleukin-2 upon stimulation with histoplasmin and yeast-phase antigens.
- Reactivity to histoplasmin decreased over time, while reactivity to yeast-phase components remained strong.
- Identified two immunodominant regions in cytosol (18-26 kDa and 35-39 kDa) and one in cell wall/membrane (35-39 kDa).
- Antigen recognition was restricted by I-Ab.
Conclusions:
- The developed T-cell hybridomas are valuable tools for dissecting the immune response to H. capsulatum.
- Specific yeast-phase antigens have been identified that trigger CD4+ T-cell activation.
Abstract:
Activation of CD4+ T cells is a crucial step in the elimination of Histoplasma capsulatum yeast cells from tissues. However, only a limited amount of information exists concerning the immunobiology of H. capsulatum-reactive T cells that are CD4+. To facilitate the analysis of the functional activities of this T-cell subpopulation, we developed a panel of 10 murine T-cell hybridomas from splenocytes of immune C57BL/6 mice. All hybridomas reacted with monoclonal anti-CD4+ antibody and released interleukin-2 after stimulation with histoplasmin. Within 3 weeks, the reactivity of hybridomas to histoplasmin declined dramatically, yet the cells responded vigorously to yeast-phase preparations that were enriched for cytosol, cell wall, or cell membrane. Of 10 hybridomas studied, only one recognized heterologous fungal antigens. Responsiveness to yeast-phase antigens was restricted by I-Ab. We mapped determinants in cytosol and cell wall or cell membrane by the technique of one-dimensional T-cell immunoblotting. The patterns of responses of hybridomas to cytosol were nearly uniform. All hybridomas responded to two immunodominant regions in cytosol with masses ranging from less than or equal to 18 to 26 kilodaltons (kDa) and 35 to 39 kDa. All hybridomas tested responded to determinants in the cell wall or cell membrane preparation with masses of 35 to 39 kDa. These hybridomas provide a useful tool for defining yeast-phase antigens that trigger T-cell activation.
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