M. Fujiki et al., Role of T cells in bronchoalveolar space in the development of interstitial pneumonia induced by superantigen in autoimmune-prone mice, AM J RESP C, 21(6), 1999, pp. 675-683
Citations number
37
Categorie Soggetti
da verificare
Journal title
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
To study the mechanisms underlying the development of interstitial pneumoni
a in autoimmune disease, we analyzed bronchoalveolar lavage fluid (BALF) in
an animal model of interstitial pneumonia in which an intratracheal instil
lation of staphylococcal enterotoxin B (SEB) induced interstitial pneumonia
in autoimmune-prone mice. Increases in the numbers of total cells, macroph
ages, lymphocytes, and neutrophils were observed in BALF from SEB-treated M
RL +/+ mice, and peaked at 3 d after SEB administration (Day 3), Flow cytom
etric analyses revealed increases in SEB-reactive V beta 8(+) T cells, indi
cating that SEB-reactive cells play an important role in bronchoalveolar sp
ace, The expressions of tumor necrosis factor (TNF)-alpha, interferon (IFN)
-gamma, JE/monocyte chemoattractant protein-1, regulated on activation, nor
mal T cells expressed and secreted, and KC/gro messenger RNA (mRNA) in BALF
cells from SEB-treated mice peaked at Day 3. Increased expression of TNF-a
mRNA was observed mainly in macrophages and CD8(+) T cells, and the increa
se in IFN-gamma mRNA was observed mainly in CD8(+) T cells in BALF at Day 3
, The expression of platelet-derived growth factor mRNA was very weak at Da
y 3 but strongly expressed at Day 14. An immunosuppressant, FK506, but not
corticosteroid, suppressed SEB-induced T-cell expansion in BALF as well as
increased cytokine and chemokine production in the bronchoalveolar space of
SEB-treated mice. Histologically, FK506 but not corticosteroid significant
ly reduced both the cell infiltration to alveolar septal walls and the synt
hesis of pulmonary collagen fibers. Further, transfer of T cells of MRL +/ mice with SEB into SCID mice gave rise to interstitial pneumonia, These re
sults suggest that superantigen-reactive T cells in the bronchoalveolar spa
ce may trigger the development of interstitial pneumonia in this model. Fuj
iki, M., T. Shinbori, M. Suga, H. Miyakawa, and M. Ando. 1999. Role of T ce
lls in bronchoalveolar space in the development of interstitial pneumonia i
nduced by superantigen in autoimmune-prone mice.