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Concanavalin A 및 방사선 조사 처리한 마우스의 면양적혈구에 대한 입양면역 : Adoptive immune response to sheep RBC in Concanavalin A treated and irradiated mouse

DC Field Value Language
dc.contributor.author장우현-
dc.contributor.author김익상-
dc.contributor.author이명수-
dc.contributor.author이승훈-
dc.date.accessioned2009-09-16T06:11:38Z-
dc.date.available2009-09-16T06:11:38Z-
dc.date.issued1981-03-
dc.identifier.citationSeoul J Med, Vol.22 No.1, pp. 67-74-
dc.identifier.issn0582-6802-
dc.identifier.urihttps://hdl.handle.net/10371/9477-
dc.description.abstractMice treated with Con A, via the same route as
that of immunization , one or two days prior to immunization
with SRBC showed a significant suppres'
sion of direct PFC response. This immunosuppressive
effect could be reversed by using higher dose of
antigen. Cotreatment of Can A-activated spleen cells
suppressed primary or secondary PFC response of the
irradiated mice adoptively transferred with normal or immunized spleen cells. Normal syngeneic recipient
mice transferred with Con A-activated spleen cells
showed a suppression of primary direct PFC response.
Recipients transfered with Con A-activated thymocytes
showed no effect on PFC response
It is suggested that Con A induced immunosuppressian
of T ·dependent humoral immune response in
mice is at least partly due to the activation of a
subpopulation of T cells, and that the effect is transferred
to syngeneic normal mice with Can A-activated
spleen cells.
-
dc.language.isoko-
dc.publisher서울대학교 의과대학-
dc.titleConcanavalin A 및 방사선 조사 처리한 마우스의 면양적혈구에 대한 입양면역-
dc.title.alternativeAdoptive immune response to sheep RBC in Concanavalin A treated and irradiated mouse-
dc.typeSNU Journal-
dc.contributor.AlternativeAuthorChang, Woo Hyun-
dc.contributor.AlternativeAuthorKim, Ik Sang-
dc.contributor.AlternativeAuthorLee, Myung Soo-
dc.contributor.AlternativeAuthorLee, Seung Hoon-
dc.citation.journaltitle서울 의대 잡지-
dc.citation.journaltitle서울 의대 학술지-
dc.citation.journaltitleSeoul Journal of Medicine-
dc.citation.endpage74-
dc.citation.number1-
dc.citation.pages67-74-
dc.citation.startpage67-
dc.citation.volume22-
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