TY - JOUR
T1 - Long-term effects of splenectomy on immunocompetent cells of adult mice
AU - Slavin, S.
AU - Zan-Bar, I.
AU - Strober, S.
N1 - Funding Information:
i This work was supported by National Institute of Health Grants AI 11313,AI 15387,and the Howard Hughes Medical Institute. 2 Present address: Department of Medicine A, Hadassah University Hospital and School of Medicine, Jerusalem, Israel. 3 Present address: Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
PY - 1980
Y1 - 1980
N2 - The long-term effects of adult splenectomy on immunocompetent cells was studied in BALB/c mice during an observation period of 600 days following splenectomy in comparison to age-matched controls. The percentage and absolute number of circulating Thy 1.2-positive (T) cells diminished gradually, reaching about 50% of the level of T cells in age-matched controls, with a concomittant increase in the proportion of Ig-positive (B) cells. The in vitro response of peripheral blood lymphocytes (PBL) to T-cell mitogens showed a 60% decrease of [3H]TdR uptake following phytohemagglutinin stimulation without a significant impairment of the responsiveness to concanavalin A. Alloreactivity of PBL was unaltered by splenectomy since both the in vitro reactivity of PBL to allogeneic cells using mixed leukocyte reaction, and the in vivo assay, measuring a first set skin allograft survival, were similar to those observed in age-matched controls. Studies on the humoral antibody responsiveness to sheep red blood cells (SRBC) indicated a diminished primary, and normal secondary anti-SRBC responses in splenectomized mice. No IgG response was detectable in mice primed with SRBC starting at 160 days following splenectomy, whereas normal IgG titers were observed following SRBC boost in splenectomized mice. We conclude that the spleen seems to play a regulatory role on some immune functions during adult life in mice.
AB - The long-term effects of adult splenectomy on immunocompetent cells was studied in BALB/c mice during an observation period of 600 days following splenectomy in comparison to age-matched controls. The percentage and absolute number of circulating Thy 1.2-positive (T) cells diminished gradually, reaching about 50% of the level of T cells in age-matched controls, with a concomittant increase in the proportion of Ig-positive (B) cells. The in vitro response of peripheral blood lymphocytes (PBL) to T-cell mitogens showed a 60% decrease of [3H]TdR uptake following phytohemagglutinin stimulation without a significant impairment of the responsiveness to concanavalin A. Alloreactivity of PBL was unaltered by splenectomy since both the in vitro reactivity of PBL to allogeneic cells using mixed leukocyte reaction, and the in vivo assay, measuring a first set skin allograft survival, were similar to those observed in age-matched controls. Studies on the humoral antibody responsiveness to sheep red blood cells (SRBC) indicated a diminished primary, and normal secondary anti-SRBC responses in splenectomized mice. No IgG response was detectable in mice primed with SRBC starting at 160 days following splenectomy, whereas normal IgG titers were observed following SRBC boost in splenectomized mice. We conclude that the spleen seems to play a regulatory role on some immune functions during adult life in mice.
UR - http://www.scopus.com/inward/record.url?scp=0018969862&partnerID=8YFLogxK
U2 - 10.1016/0008-8749(80)90175-6
DO - 10.1016/0008-8749(80)90175-6
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:0018969862
SN - 0008-8749
VL - 55
SP - 444
EP - 455
JO - Cellular Immunology
JF - Cellular Immunology
IS - 2
ER -