Rj. Wilkinson et al., PEPTIDE-SPECIFIC T-CELL RESPONSE TO MYCOBACTERIUM-TUBERCULOSIS - CLINICAL SPECTRUM, COMPARTMENTALIZATION, AND EFFECT OF CHEMOTHERAPY, The Journal of infectious diseases, 178(3), 1998, pp. 760-768
The T cell repertoire of 59 patients with untreated tuberculosis was c
ompared with that of 46 bacille Calmette-Guerin-vaccinated controls by
assaying the proliferative responses to six permissively recognized p
eptides from the 16-, 19-, and 38-kDa molecules of Mycobacterium tuber
culosis. A trend from higher to lower reactivity following this order:
vaccinated controls > lymph node disease > localized extrapulmonary >
pulmonary > pleural was seen for 4 of the peptides (P <.03), The decr
eased response of blood lymphocytes from patients with pleural tubercu
losis was partially accounted for by sequestration of peptide-responsi
ve cells within the pleural fluid, Chemotherapy ''reversed'' the depre
ssed proliferative responses of patients with pulmonary and pleural tu
berculosis depending on the peptide origin, being greatest for peptide
s of 16 kDa, transient for those of 19 kDa, and least for those of 38
kDa, These data demonstrate antigen specificity in the decreased respo
nsiveness of patients with tuberculosis.