TY - JOUR
T1 - Interstitial pneumonitis during murine cytomegalovirus infection and graft-versus-host reaction
T2 - Characterization of bronchoalveolar lavage cells
AU - Shanley, John D.
AU - Via, Charles S.
AU - Sharrow, Susan O.
AU - Shearer, Gene M.
PY - 1987/11
Y1 - 1987/11
N2 - Acute murine cytomegalovirus (MCMV) infection alters the course of graft-vs-host (GVH) disease involving major histocompatibility (MHC) antigens and induces interstitial pneumonitis. F1 (B10xB10.BR) mice given 20x106 B10.BR spleen cells and MCMV (1x105 plaque-forming units [PFU]) develop severe, diffuse pneumonitis not seen with either MCMV or GVH alone. As one index of the host immune processes operating in the lungs during MCMV/GVH pneumonitis, we examined the types of cells recovered from the lung by bronchoalveolar lavage (BAL) during pneumonitis. During MCMV/GVH pneumonitis, the total cells recovered significantly increased, due primarily to an influx of Thy 1.2 lymphocytes. Characterization of cells using multiparameter flow cytometric analysis revealed that >80% of all BAL cells were Thy 1.2-positive lymphocytes of donor origin. In addition, donor Thy 1.2-positive cells were of both the L3T4+ (43% of BAL cells) and Lyt 2+ (38% of BAL cells) phenotype. Thus, MCMV infection during GVH to MHC antigens induces interstitial pneumonitis, characterized by an influx of T lymphocytes (both helper and suppressor/cytotoxic) from the donor. The antigenic specificity of these cells is not known.
AB - Acute murine cytomegalovirus (MCMV) infection alters the course of graft-vs-host (GVH) disease involving major histocompatibility (MHC) antigens and induces interstitial pneumonitis. F1 (B10xB10.BR) mice given 20x106 B10.BR spleen cells and MCMV (1x105 plaque-forming units [PFU]) develop severe, diffuse pneumonitis not seen with either MCMV or GVH alone. As one index of the host immune processes operating in the lungs during MCMV/GVH pneumonitis, we examined the types of cells recovered from the lung by bronchoalveolar lavage (BAL) during pneumonitis. During MCMV/GVH pneumonitis, the total cells recovered significantly increased, due primarily to an influx of Thy 1.2 lymphocytes. Characterization of cells using multiparameter flow cytometric analysis revealed that >80% of all BAL cells were Thy 1.2-positive lymphocytes of donor origin. In addition, donor Thy 1.2-positive cells were of both the L3T4+ (43% of BAL cells) and Lyt 2+ (38% of BAL cells) phenotype. Thus, MCMV infection during GVH to MHC antigens induces interstitial pneumonitis, characterized by an influx of T lymphocytes (both helper and suppressor/cytotoxic) from the donor. The antigenic specificity of these cells is not known.
UR - http://www.scopus.com/inward/record.url?scp=0023502012&partnerID=8YFLogxK
U2 - 10.1097/00007890-198711000-00013
DO - 10.1097/00007890-198711000-00013
M3 - Article
C2 - 2446406
AN - SCOPUS:0023502012
SN - 0041-1337
VL - 44
SP - 658
EP - 662
JO - Transplantation
JF - Transplantation
IS - 5
ER -