Separation of Helper a N D Suppressor T Lymphocytes

نویسنده

  • RICHARD W. DUTTON
چکیده

The existence of subpopulations of T cells has been recognized in a number of experimental models. Raft and Cantor (1) first subdivided T cells into T1 and T2 according to an antigen-driven maturation scheme. T1 cells which were immature, short-lived, and noncirculating upon encounter with antigens developed into mature T~ cells which were long-lived, circulating, and had a lower density of Thy-1 antigen on the cell surface. More recently it would appear that the T1 and T2 progression may occur in a number of parallel T-cell subpopulations and it may be more appropriate to subdivide T cells on a functional basis into TN, the helper cells carrying Ly-1 antigens and Tc.s, the cytotoxic and suppressor T cells carrying the Ly-2,3 antigens (references 2-4 and H. Cantor, personal communication). Although cytotoxic and suppressor T cells have been separately detected in many different systems (5-8), their relationship to each other remains unclear and they are tentatively grouped together. It should also be noted that cell cooperation is not limited to Tand B-cell systems. Collaboration between T-cell subpopulations in the generation of effector T cells has been suggested in a number of experimental systems (e.g. Asofsky et al. (9); Bach and Bach (10)). While the helper and cytotoxic functions of T cells are now more or less established concepts (5, 11), the functional role of T-suppressor cells is less well defined. Gershon (6) was among the first to observe that cells from mice made tolerant to sheep erythrocytes (SRBC) when transferred to normal mice conferred tolerance on the recipient. This "infectious" phenomenon could be completely abrogated by anti-0 treatment. In other systems, Herzenberg and Herzenberg (12), Baker et al. (13), Tada and Takemori (14), Rich and Pierce (7), and Dutton (15) provide further evidence for the existence of suppressor cells. On the other hand, Coutinho and M611er (16) have proposed a "one nonspecific signal hypothesis" and suggested that suppression is merely due to too much help. The answer as to whether helper and suppressor T cells are distinct subpopulations will help resolve this dilemma. We have previously shown that the incubation of mouse spleen cells with concanavalin A (Con A) ~ induced both helper and suppressor activities for the

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

Separation of helper and suppressor T lymphocytes on a ficoll velocity sedimentation gradient

A 5-20% Ficoll velocity sedimentation gradient has been successfully applied to separate concanavalin A (Con A)-induced helper; and suppressor T cells. When titrated into a constant number of fresh normal spleen cells responding to sheep erythrocytes, cells from the top pool show stimulatory effects while those from the bottom pool show inhibitory activity. Both activities are found to be Con A...

متن کامل

Regulatory functions of hapten-reactive helper and suppressor T lymphocytes. II. Selective inactivation of hapten-reactive suppressor T cells by hapten-nonimmunogenic copolymers of D-amino acids, and its application to the study of suppressor T-cell effect on helper T-cell development

An experimental condition was established in vivo for selectively eliminating hapten-reactive suppressor T-cell activity generated in mice primed with a para-azobenzoate (PAB)-mouse gamma globulin (MGG)-conjugate and treated with PAB-nonimmunogenic copolymer of D-amino acids (D- glutamic acid and D-lysine; D-GL). The elimination of suppressor T-cell activity with PAB-D-GL treatment from the mix...

متن کامل

Separation of helper and suppressor T lymphocytes. II. Ly phenotypes and lack of DNA synthesis requirement for the generation of concanavalin A helper and suppressor cells

Using a Ficoll velocity sedimentation gradient, we have been able to fractionate concanavalin A (Con A)-induced helper and suppressor cells into separate pools. Cells activated by Con A to mediate helper activity are Ly1+, do not require DNA synthesis for induction, and remain as small cells after activation. Suppressor cells are Ly23+, are found in the blast cell fraction and their induction i...

متن کامل

The mechanism of tolerance induction in thymus-derived lymphocytes; I. intracellular inactivation of hapten-reactive helper T lymphocytes by hapten-nonimmunogenic copolymer of D-amino acids

Treatment of a p-azobenzoate (PAB) derivative of a copolymer of D-glutamic acid and D-lysine (D-GL) induced a profound state of unresponsiveness to PAB-reactive helper T lymphocytes generated in PAB-mouse gamma globulin (MGG)-primed mice. This unresponsiveness in T lymphocytes was specific for PAB-reactive cells, since the bacterial alpha-amylase-, keyhole limpet hemocyanin-, or ovalbumin-prime...

متن کامل

SEPARATION OF HELPER T CELLS FROM SUPPRESSOR T CELLS EXPRESSING DIFFERENT Ly COMPONENTS I. Polyclonal Activation: Suppressor and Helper Activities are Inhe

Peripheral T lymphocytes can be subclassified on the basis of differential expression of Ly components on their surfaces (1-3). Approximately 50% of peripheral T cells manifest all three Ly components analyzed so far (phenotype Ly123), about 33% only Lyl (phenotype Lyl), and about 5-10% Ly2 and Ly3 (phenotype Ly23). Functional studies indicate that Lyl T cells can generate helper function durin...

متن کامل

Regulatory functions of hapten-reactive helper and suppressor T lymphocytes. III. Amplification of a generation of tumor-specific killer T-lymphocyte activities by suppressor T-cell-depleted hapten- reactive T lymphocytes

2,4.6-trinitrophenyl (TNP)-reactive T-cell activities were raised in mice by immunization with TNP-isologous mouse gamma globulin. After establishing that TNP-reactive T lymphocytes can serve as amplifier cells for induction of killer T lymphocytes in allogeneic system, we explored the possibility of this hapten-reactive T-cell system to amplify tumor-specific killer T-lymphocyte activity in th...

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:

دوره   شماره 

صفحات  -

تاریخ انتشار 2003