A. Plebani et al., T-CELL ACTIVITY AND CYTOKINE PRODUCTION IN X-LINKED AGAMMAGLOBULINEMIA - IMPLICATIONS FOR VACCINATION STRATEGIES, International archives of allergy and immunology, 114(1), 1997, pp. 90-93
In the 5 X-linked agammaglobulinelnia (XLA) patients studied we show t
hat memory T cells are present and that T lymphocytes proliferate norm
ally to mitogens, monoclonal antibodies and, in particular, to recall
antigens demonstrating normal in vivo T cell priming despite the absen
ce of B cells. Furthermore, in vitro T cell activation in response to
both T cell receptor-independent and T-cell receptor-dependent signals
leads to a pattern of cytokine production characteristic of primed T
cells and necessary for normal T cell function. These data are in good
agreement with results obtained in gene-targeted mice and further sup
port the concept that the absence of B cells does not impair induction
of in vivo T cell memory and effector function which is generally con
sidered to be of great importance in conferring protection against vir
al infections. Thus, while there is no risk of inducing infections in
XLA patients by administering vaccines containing killed viruses or re
combinant viral proteins, stimulation of T cell immunity by such vacci
nes may be of potential benefit particularly in the defense against in
fections with viruses such as the hepatitis B virus to which hypogamma
globulinemic patients are particularly exposed.