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Generation of Suppressor Cells in Mice After Surgical Trauma

Overview
Journal J Clin Invest
Specialty General Medicine
Date 1980 Aug 1
PMID 6447165
Citations 18
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Abstract

Immunoincompetency is often seen in patients after various types of trauma and is associated with increased morbidity and mortality from infectious complications. To understand better the immunologic impairment associated with trauma, we have studied this phenomenon in an animal model. Splenocytes from mice traumatized by amputation of their right hind limbs were consistently shown to have a diminished capacity to proliferate in response to alloantigens and to form alloreactive cytolytic cells in mixed lymphocyte cultures. Anesthesia itself had no effect in this system. The immunoincompetency was detected from 2 h to 6 d after surgical trauma and was completely reversed by removing adherent and phagocytic cells from the splenocytes. Furthermore, addition of splenocytes from traumatized mice to mixed lymphocyte cultures from normal mice prevented normal lymphocytes from responding to alloantigens, suggesting the existence of suppressor cells. The suppressor cells were found to adhere to glass and to nylon wool columns, and were contained within an esterase-positive cell population. They were insensitive to treatment with anti-Thy 1.2 and anti-Ig sera in the presence of complement. Therefore, the present results suggest that a Thy 1.2-negative, Ig-negative, esterase-positive cell population capable of adhering to glass and nylon wool, presumably macrophages, was responsible for the inhibition of the responsiveness of lymphocytes to alloantigens in traumatized animals.

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References
1.
Constantian M . Association of sepsis with an immunosuppressive polypeptide in the serum of burn patients. Ann Surg. 1978; 188(2):209-15. PMC: 1396754. DOI: 10.1097/00000658-197808000-00014. View

2.
CHAMBLER K, Batchelor J . Influence of defined incompatibilities and area of burn on skin-homograft survival in burned-subjects. Lancet. 1969; 1(7584):16-8. DOI: 10.1016/s0140-6736(69)90984-2. View

3.
Ottesen E . Modulation of the host response in human schistosomiasis. I. Adherent suppressor cells that inhibit lymphocyte proliferative responses to parasite antigens. J Immunol. 1979; 123(4):1639-44. View

4.
Zembala M, Mytar B, Popiela T, Asherson G . Depressed in vitro peripheral blood lymphocyte response to mitogens in cancer patients: the role of suppressor cells. Int J Cancer. 1977; 19(5):605-13. DOI: 10.1002/ijc.2910190503. View

5.
MARKLEY K, SMALLMAN E, LaJohn L . The effect of thermal trauma in mice on cytotoxicity of lymphocytes. Proc Soc Exp Biol Med. 1977; 154(1):72-7. DOI: 10.3181/00379727-154-39607. View