Restoration of immunogenicity to passenger cell-depleted kidney allografts by the addition of donor strain dendritic cells

نویسندگان

  • R I Lechler
  • J R Batchelor
چکیده

The immunogenicity of long-surviving, enhanced (AS X AUG)F1 renal allografts retransplanted into secondary AS recipients was restored by the injection of small numbers of donor strain dendritic cells derived from afferent lymph. Whereas 1 X 10(4) to 5 X 10(4) dendritic cells were able to trigger an acute rejection response, neither the passenger volume of donor strain blood nor 5 X 10(6) T or B lymphocytes were able to do so, thereby demonstrating more than a 100-fold difference in immunogenic potency. It is concluded that intrarenal dendritic cells provide the major immunogenic stimulus of a kidney allograft. These results suggest that the antigenic strength of major histocompatibility complex-incompatible tissue correlates with the content of donor strain dendritic cells. They also provide further evidence that antigens of the major histocompatibility complex behave like conventional antigens unless they are on the surface of allogeneic dendritic cells.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

1836 Passenger Cells in Rat Kidney

It has already been shown (1, 2) that long-surviving, passively enhanced (AS × AUG)F1 rat kidneys originally transplanted to AS strain recipients are not rejected acutely if retransferred to a normal second AS recipients. This contrasts with the fate of normal (AS × AUG)F1 primary kidney allografts transplanted to AS recipients that are always rejected within 12 d, and suggests that in this str...

متن کامل

Critical requirement for graft passenger leukocytes in allograft tolerance induced by donor blood transfusion.

Tolerance to a vascularized allograft can be induced in adult animals by pregraft donor-specific blood transfusion (DST). Mechanisms underlying this effect appear to depend on unresponsiveness of alloreactive T-helper cells. In this study, we examined the roles of DST and cellular components of the allograft that are important in inducing T-cell unresponsiveness in a rat model. DST alone did no...

متن کامل

RAPID COMMUNICATION Critical Requirement for Graft Passenger Leukocytes in Allograft Tolerance Induced by Donor Blood Transfusion

Tolerance to a vascularized allograft can be induced in adult animals by pregraft donor-specific blood transfusion (DST). Mechanisms underlying this effect appear to depend on unresponsiveness of alloreactive T-helper cells. In this study, we examined the roles of DST and cellular components of the allograft that are important in inducing T-cell unresponsiveness in a rat model. DST alone did no...

متن کامل

Immunogenicity of retransplanted rat kidney allografts. Effect of inducing chimerism in the first recipient and quantitative studies on immunosuppression of the second recipient

It has been previously shown that long surviving, enhanced (AS X AUG)F1 rat kidneys residing in a primary AS recipient are not acutely rejected if transferred into a second AS recipient. The reduced immunogenicity of the retransplanted graft was attributed to a depletion of incompatible passenger cells. It is shown here that if the primary AS recipient is made chimeric by x irradiation and inje...

متن کامل

MHC-incompatible rat kidney grafts, when retranspIanted from a primary to a secondary recipient of the same genotype, do not elicit strong primary T-dependent alloimmunity in the secondary recipient. In contrast, normal primary kidney allografts

The question as to why major histocompatibility complex (MHC) a antigens are uniquely powerful primary immunogens and in this respect differ from antigens of the minor systems has not yet been clearly answered. A number of suggestions have been made in the past (1-3), but they have not taken into account the remarkable variation in strength with which MHC antigens induce primary, T-dependent re...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • The Journal of Experimental Medicine

دوره 155  شماره 

صفحات  -

تاریخ انتشار 1982