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Cellular Immune Responses to Four Doses of Percutaneous Bacille Calmette-Guerin in Healthy Adults
Author(s) -
Philip W. Lowry,
Thomas Ludwig,
Julie A. Adams,
M.L. Fitzpatrick,
Sabrina Grant,
G A Andrle,
M R Offerdahl,
S N Cho,
David R. Jacobs
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/515614
Subject(s) - vaccination , immune system , immunology , medicine , immunization , immunity , lymphoproliferative response , tuberculosis , antigen , bcg vaccine , dose , mycobacterium tuberculosis , delayed hypersensitivity , cellular immunity , biology , in vitro , pathology , peripheral blood mononuclear cell , biochemistry
To explore the hypothesis that low-dose immunization might induce preferential Th1 cell immunity, 76 adults were vaccinated with one of four doses of bacille Calmette-Guérin (BCG): The doses contained very low (1.6 x 10(5) cfu), low (3.2 x 10(6) cfu), standard (1.6 x 10(8) cfu), or high (3.2 x 10(8) cfu) levels of BCG. Delayed-type hypersensitivity responses occurred 8 weeks after vaccination in 10% of persons given very low or low doses of BCG, compared with 95% and 100% of persons given standard or high doses, respectively. Lymphoproliferative responses, which were increased only for high-dose vaccinees, peaked 2 weeks after vaccination and were directed chiefly against Mycobacterium tuberculosis-secreted proteins, particularly the antigen 85 complex. Significant increases in mycobacteria-specific interferon-gamma expression were present 16 weeks after vaccination only for persons given standard or high doses of BCG. Percutaneous BCG appears capable of inducing a temporary Th1-like immune response, but standard or higher dosages are required.

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