Me. Hilburger et Bs. Zwilling, ANTIGEN PRESENTATION BY MACROPHAGES FROM BACILLE CALMETTE-GUERIN (BCG)-RESISTANT AND (BCG)-SUSCEPTIBLE MICE, Clinical and experimental immunology, 96(2), 1994, pp. 225-229
We have compared the antigen-presenting capacity of macrophages from c
ongenic BALB/c.Bcg(r) and BALB/c.Bcg(s) mice that differentially expre
ss MHC class II glycoproteins. Several different criteria were used to
evaluate the presentation of a protein antigen, ovalbumin (OVA), incl
uding limiting the concentration of antigen or the numbers of macropha
ges, and using both native OVA and OVA peptide 323-339. No differences
in the capacity of macrophages from Bcg(r) and Bcg(s) mice to present
antigen to a OVA-specific T cell hybridoma were found. Splenic macrop
hages from BCG-infected congenic mice also induced an equivalent amoun
t of IL-2 production by the T cell hybridoma. The relationship of thes
e findings to other differences that have been attributed to Bcg are d
iscussed.