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My laboratory is focused on
understanding the mechanisms of pulmonary immunity and pulmonary fibrosis
and on studying the regulation and development of anti-leukemic activity
in syngeneic graft versus-host disease.
Experiments from our laboratory were
the first to show that BLM-induced pulmonary fibrosis could be induced in
SCID mice in the absence of lymphocytes and that fibrosis under those
conditions were associated with profound eosinophilia. More recent studies
have shown that BLM-induced fibrosis occurred in anti-IL-5 knockout mice
in the absence of eosinophilia as well as in NK deficient mice suggesting
that neither cell type was required for the induction of fibrosis.
Currently, the levels and kinetics of fibrogenic and anti-inflammatory
cytokines are being elucidated to determine their role in fibrosis. In
addition, we have adopted a transgenic mouse strategy to deplete monocytes
and consequently inflammatory macrophages by expressing an inducible
suicide gene for the macrophage specific promoter, cfms, to express green
fluorescent protein (GFP) and a suicide gene containing two units of FK506
binding protein (FKBP) fused to the cytoplasmic region of Fas.
Dimerization of the FKBP with the drug AP20187 activates fas-mediated
apoptosis and results in a dramatic reduction in GFP+ macrophages.
In addition, these Tg mice develop an interesting clinical syndrome
that includes massive adhesions and inflammation, the mechanism of which
is currently under study.
We are also studying the mechanisms
responsible for the induction of murine cyclosporine A-induced syngeneic
graft-versus-host disease (SGVHD). Ongoing work in this model has ranged
from describing the regulation and pathogenesis associated with the
induction and adoptive transfer of this disease, to analysis of T cell
clones isolated from diseased animals. It has been shown clinically that a
beneficial consequence of GVHD following bone marrow transplantation (BMT)
is the generation of anti-tumor or graft-versus-leukemia (GVL) responses
and similarly mice with SGVHD have demonstrated the ability to reject
syngeneic tumors. We are currently studying three aspects of SGVHD: 1) the
immunoregulatory events that are responsible for induction of the disease;
2) the mechanism of GVL activity with particular focus on innate immunity;
and 3) the induction and regulation of a Crohn’s/colitis like autoimmune
disease which appears to be a prominent feature of SGVHD.
Selected Publications
Lake-Bullock, H.V., Bryson, J.S., Jennings, C.D., Kaplan, A.M.
Inhibition of graft-versus-host disease: Use of a T-cell controlled
suicide gene. J. Immunol. 158:5079-5082, 1997.
Bryson, J.S., Jennings, C.D., Lowery, D.M., Carlson, S.L., Pflugh, D.L.,
Caywood, B.E. and Kaplan, A.M. Rejection of an MHC Class II
negative tumor following induction of murine syngeneic graft-versus-host
disease. Bone Marrow Transplantation 23:363-372, 1999.
Lake-Bullock, H.V., Zhu, J., Hao, J., Cohen, D.A., and Kaplan, A.M.
T Cell Independence of Bleomycin-Induced Pulmonary Fibrosis. J. Leukocyte
Biology 65:187-195, 1999.
Hao, H., Cohen, D.A., Jennings, C.D.,
Bryson, S.J., and Kaplan, A.M.
Lack of a role of eosinophils in bleomycin-induced pulmonary
fibrosis. J. Leukocyte Biol. 68:515-521, 2000.
Avduishko,
R., Hongo, D., Lake-Bullock, H., Kaplan,
A.M. and Cohen, D.A. IL-10
receptor dysfunction in macrophages during chronic inflammation.
J. Leukocyte Biol., 70:624-632, 2001.
Lowery-Flanagan,
D.M., Gross, R., Jennings, C.D., Caywood, B.E., Goes, S., Kaplan,
A.M. and Bryson, J.S. Induction of syngeneic graft-versus-host disease
in LPS hyporesponsive C3H/HeJ mice. J.
Leukocyte Biol. 70:873-880,
2001.
Lower
Flanagan, D.M., Jennings, C.D., Caywood, B.E., Gross, R., Goes, S., Kaplan,
A.M. and Bryson, J.S. Nitric
oxide mediates intestinal pathology of murine cyclosporine-induced
syngeneic-graft-versus-host disease.
J. Leukocyte Biology. 72:762-768, 2002.
Fernandez, S., Jose, P.,
Avdiushko, M., Kaplan, A.M. and Cohen, D.A. Inhibition of IL-10
receptor function in the lung by Toll-Like receptor agonists. Submitted.
Bryson,
J.S., Zhang, L., Goes, S.W., Jennings, C.D., Caywood, B.E., Carlson, S.L.
and Kaplan, A.M. CD4+ T cells mediate murine syngeneic
graft-versus-host disease-associated colitis. Submitted
Burnett,
S., Zhang, J., Kaplan, A.M., and Cohen, D.A. Conditional macrophage
ablation in transgenic mice expressing a Fas-based suicide gene. In
preparation.
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