Kj. Parlevliet et al., EFFECTS OF ANTI-CD3 MONOCLONAL-ANTIBODIES ON FUNCTIONAL-ACTIVITY OF LYMPHOCYTES - STUDIES IN-VIVO AND IN-VITRO, Clinical and experimental immunology, 99(2), 1995, pp. 155-159
Lymphocyte functional activity was tested in 38 renal transplant recip
ients receiving induction treatment with various anti-CD3 MoAbs, i.e.
OKT3, T3.G2a (an IgG2a anti-CD3 MoAb) or T3.A (an IgA anti-CD3 MoAb of
the same idiotype). During treatment with OKT3 and T3.G2a, lymphocyte
response to phytohaemagglutinin-P (PHA), as determined with the use o
f a whole-blood lymphocyte culture technique, decreased significantly.
However, during treatment with T3.A PHA response was not affected. Us
ing a conventional lymphocyte culture technique, PHA response was unch
anged during treatment with all three MoAbs, indicating that the immun
osuppressive effect of OKT3 and T3.G2a is probably dependent upon the
presence of MoAb in culture medium and is reversible. In addition, we
tested in vitro inhibition of aspecific mitogen- or antigen-induced ly
mphocyte stimulation by OKT3, T3.A and T3.G2a. It appeared that at low
concentrations (< 25 ng/ml) T3.G2a and OKT3 exerted a stronger immuno
suppressive effect than T3.A. However, at higher concentrations T3.A,
OKT3 and T3.G2a were equally immunosuppressive. We conclude that the i
mmunosuppressive effect of T3.A is caused by blindfolding. At low conc
entrations T3.G2a exerts its immunosuppressive effect mainly through m
odulation of the CD3 and/or T cell receptor complex, as a result of in
teraction with Fc receptors on monocytes. At higher concentrations bli
ndfolding of the CD3/T cell receptor complex may contribute to immunos
uppression.