Article
Peripheral blood mononuclear cells from individuals infected with human T-cell lymphotropic virus type 1 have a reduced capacity to respond to recall antigens
Registro en:
MASCARENHAS, R. E. et al. Peripheral blood mononuclear cells from individuals infected with human T-cell lymphotropic virus type 1 have a reduced capacity to respond to recall antigens. Clinical and Vaccine Immunology, v. 13, n. 5, p. 547-552, 2006.
1556-6811
10.1128/CVI.13.5.547–552.2006
Autor
Mascarenhas, Rita Elizabeth Moreira
Brodskyn, Claudia Ida
Barbosa, Geisa
Clarêncio, Jorge
Andrade Filho, Antonio de Souza
Figueiroa, Frederico
Castro Filho, Bernardo Galvão
Grassi, Maria Fernanda Rios
Resumen
Evidence indicates that human T-cell lymphotropic virus type 1 (HTLV-1) infection leads to chronic
immunosuppression and a greater susceptibility to infectious diseases. Spontaneous in vitro proliferation of
peripheral blood mononuclear cells (PBMC) is an important immunological feature of HTLV-1-infected
individuals. However, the association between spontaneous proliferation and immunosuppression is not clear.
In this study, we evaluated the cellular immune responses of PBMC from 58 asymptomatic HTLV-1-infected
individuals with PBMC showing or not showing spontaneous proliferation. Individuals with PBMC that
spontaneously proliferated had increased proportions of CD4 T cells expressing CD45RO and dramatically
reduced responses to recall antigens. In addition, frequencies of positive responses to recall antigens were also
decreased in HTLV-infected individuals without spontaneous proliferation of PBMC. There was a polyclonal
expansion of multiple T-cell receptor V families of CD4 T lymphocytes in patients with spontaneous
proliferation. We observed that HTLV-1 induced an immunosuppression characterized by a decrease in the
stimulation index to a recall antigen, even in individuals who did not present spontaneous proliferation. On the
other hand, only patients with PBMC presenting spontaneous proliferation showed polyclonal activation and
increased proportion of CD4 T cells expressing CD45RO.
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