Prolonged survival of mouse skin allografts in recipients treated with donor splenocytes and antibody to CD40 ligand

被引:137
作者
Markees, TG
Phillips, NE
Noelle, RJ
Shultz, LD
Mordes, JP
Greiner, DL
Rossini, AA
机构
[1] UNIV MASSACHUSETTS, SCH MED, DIV DIABET, BIOTECH 2, WORCESTER, MA 01605 USA
[2] DARTMOUTH COLL SCH MED, DEPT MICROBIOL, LEBANON, NH 03765 USA
[3] JACKSON LAB, BAR HARBOR, ME 04609 USA
关键词
D O I
10.1097/00007890-199707270-00026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Combined treatment with antibody against CD40 ligand and one transfusion of donor splenocytes prolonged survival of fully mismatched BALB/c skin allografts on C57BL/6 recipients, with similar to 20% of grafts surviving >100 days. In vitro alloresponsiveness in treated animals was reduced in the immediate posttransplantation period, but by day 100 was increased despite the presence of a successful allograft. The presence of alloreactivity on day 100 was confirmed in vivo by adoptive transfer, which suggests that our protocol had induced either a state of ''split tolerance'' or ''graft accommodation.'' Mice with skin grafts that had survived for greater than or equal to 100 days revealed no evidence of lymphoid chimerism. Treatment with donor splenocytes and antibody against CD40 ligand permits longterm survival of highly antigenic donor skin allografts despite the presence of functionally intact alloreactive lymphocytes.
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收藏
页码:329 / 335
页数:7
相关论文
共 59 条
[11]   PREVENTION OF ALLOGRAFT-REJECTION BY IMMUNIZATION WITH DONOR BLOOD DEPLETED OF IA-BEARING CELLS [J].
FAUSTMAN, D ;
LACY, P ;
DAVIE, J ;
HAUPTFELD, V .
SCIENCE, 1982, 217 (4555) :157-158
[12]   SUBSETS OF CD4+ T-CELLS AND THEIR ROLES IN THE INDUCTION AND PREVENTION OF AUTOIMMUNITY [J].
FOWELL, D ;
MCKNIGHT, AJ ;
POWRIE, F ;
DYKE, R ;
MASON, D .
IMMUNOLOGICAL REVIEWS, 1991, 123 :37-64
[13]   IN-VIVO CD40-GP39 INTERACTIONS ARE ESSENTIAL FOR THYMUS-DEPENDENT HUMORAL IMMUNITY .2. PROLONGED SUPPRESSION OF THE HUMORAL IMMUNE-RESPONSE BY AN ANTIBODY TO THE LIGAND FOR CD40, GP39 [J].
FOY, TM ;
SHEPHERD, DM ;
DURIE, FH ;
ARUFFO, A ;
LEDBETTER, JA ;
NOELLE, RJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1567-1575
[14]   Immune regulation by CD40 and its ligand GP39 [J].
Foy, TM ;
Aruffo, A ;
Bajorath, J ;
Buhlmann, JE ;
Noelle, RJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :591-617
[15]   STRONG T-CELL TOLERANCE IN PARENT-]F1 BONE-MARROW CHIMERAS PREPARED WITH SUPRALETHAL IRRADIATION - EVIDENCE FOR CLONAL DELETION AND ANERGY [J].
GAO, EK ;
LO, D ;
SPRENT, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (04) :1101-1121
[16]   A central role of CD40 ligand in the regulation of CD4(+) T-cell responses [J].
Grewal, IS ;
Flavell, RA .
IMMUNOLOGY TODAY, 1996, 17 (09) :410-414
[17]   Identification of a costimulatory molecule rapidly induced by CD40L as CD44H [J].
Guo, Y ;
Wu, Y ;
Shinde, S ;
Sy, MS ;
Aruffo, A ;
Liu, Y .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (03) :955-961
[18]   ANTIGEN PRESENTATION BY CHEMICALLY MODIFIED SPLENOCYTES INDUCES ANTIGEN-SPECIFIC T-CELL UNRESPONSIVENESS INVITRO AND INVIVO [J].
JENKINS, MK ;
SCHWARTZ, RH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 165 (02) :302-319
[19]   TOLERANCE OF CD8+ T-CELLS DEVELOPING IN PARENT -] F1-CHIMERAS PREPARED WITH SUPRALETHAL IRRADIATION - STEP-WISE INDUCTION OF TOLERANCE IN THE INTRATHYMIC AND EXTRATHYMIC ENVIRONMENTS [J].
KOSAKA, H ;
SPRENT, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (02) :367-378
[20]   Functions of CD40 and its Ligand, gp39 (CD40L) [J].
Laman, JD ;
Claassen, E ;
Noelle, RJ .
CRITICAL REVIEWS IN IMMUNOLOGY, 1996, 16 (01) :59-108