EVOLVING T-CELL RESPONSES IN MURINE SCHISTOSOMIASIS - TH2 CELLS MEDIATE SECONDARY GRANULOMATOUS HYPERSENSITIVITY AND ARE REGULATED BY CD8-CELLS IN-VIVO( T)
Sw. Chensue et al., EVOLVING T-CELL RESPONSES IN MURINE SCHISTOSOMIASIS - TH2 CELLS MEDIATE SECONDARY GRANULOMATOUS HYPERSENSITIVITY AND ARE REGULATED BY CD8-CELLS IN-VIVO( T), The Journal of immunology, 151(3), 1993, pp. 1391-1400
The dynamics of T cell maturation and regulation were examined during
the granulomatous response to Schistosoma mansoni eggs under condition
s of primary (PRIM), secondary vigorous (VIG), and secondary immunomod
ulated (MOD) immunity. The patterns of VIG and MOD GR (GR) formation w
ere established in naive CBA mice by transfer of lymphoid cells from S
. mansoni-infected donors at the VIG and MOD stages of infection. Sequ
ential production of IFN, IL-2, and IL-4 was assessed at the GR and in
draining lymph nodes (LN) to determine the participation of Th1 (IFN-
producing) and Th2 (IL-4/IL-5-producing) cells. The PRIM GR produced I
FN in the growth phase (2-16 days) and IL-4 was detected only after le
sions were established (16-24 days). The PRIM LN showed coincident pro
duction of IFN, IL-2, and IL-4 on day 4 followed by mainly IL-4 and IL
-2 production on day 8, consistent with Th2 differentiation via a Th0
precursor. The VIG GR produced high levels of IL-4 in the growth phase
(4-8 days) although IFN remained at modest levels. The VIG LN showed
increased cytokine levels consistent with an anamnestic response and a
gain the pattern suggested Th2 differentiation from Th0 cells. The MOD
mice had abrogated GR IL-4 levels and arrested Th2 differentiation in
LN. In vitro mix studies indicated that the impaired cytokine product
ion was not due to direct suppression. The role of Ts cells was next e
xplored by T cell subset depletion. Pan-T cell depletion of VIG cells
profoundly abrogated IL-4 production although CD8+ cell depletion augm
ented GR area by 70% as well as local and regional IL-4 production by
100 to 150%. Similarly, CD8+ cell depletion of MOD cells augmented GR
size and IL-4 production but the response was less than corresponding
VIG mice, suggesting that Th activity was reduced in MOD mice. Transfe
r studies indicated that CD8+ cells inhibited Th2 maturation in LN. Th
us, the schistosome egg GR demonstrated a Th1-like pattern in the PRIM
response followed by a Th2 pattern in the VIG stage and abrogated Th2
activity in the MOD stage. Finally, the phenomenon of ''spontaneous m
odulation'' likely represents the cumulative action of CD8+ cells whic
h steadily erode the Th population.