Immunomodulatory activity of different blood products on the mitogen-induced human lymphocyte transformation

Transfus Med. 1992 Sep;2(3):215-21. doi: 10.1111/j.1365-3148.1992.tb00158.x.

Abstract

Blood transfusions have an immunosuppressive effect on the recipient and induce changes in several immunological parameters. We studied the effect of homologous and autologous fresh plasma (FP), fresh frozen plasma (FFP), heparinized plasma, as well as the influence of red blood cells (RBC), CPDA-1, CPD, heparin, PAGGS-mannitol, SAG-mannitol and ADSOL on mitogen-induced lymphocyte transformation. Both homologous and autologous FP and FFP decreased the PHA and ConA response of human lymphocytes (P < 0.05). The PWM response was reduced by FP (P < 0.05). The mean t1/2 of plasma-induced suppression was approximately 38 h. Dose-dependent suppression rates were observed with pure CPDA-1 and CPD solutions. In contrast, heparinized plasma showed an elevated PHA- and ConA-induced transformation rate (P < 0.025), whereas PWM induction was unaffected. In addition, washed RBC, pure PAGGS-M, SAG-M and ADSOL solutions revealed no effect on the PHA response. Freezing, heating or recalcification of plasma resulted in an increase in the PHA response. Adenine was not immunosuppressive in vitro. We conclude that, in addition to unspecific mechanisms by CPDA-1 or CPD, an unknown plasma factor, which is susceptible to changes in temperature or storage conditions, suppresses the PHA-, PWM- or ConA-induced T-cell immune response. Further clinical studies are needed to correlate these observations with clinical phenomena.

Publication types

  • Comparative Study

MeSH terms

  • Adenine / pharmacology
  • Adjuvants, Immunologic / pharmacology*
  • Antibody Formation
  • Calcium / pharmacology
  • Cells, Cultured
  • Concanavalin A / pharmacology
  • Erythrocytes / physiology*
  • Freezing
  • Heparin / pharmacology
  • Hot Temperature
  • Humans
  • Lymphocyte Activation*
  • Mitogens*
  • Phytohemagglutinins / pharmacology
  • Plasma / physiology*
  • Solutions

Substances

  • Adjuvants, Immunologic
  • Mitogens
  • Phytohemagglutinins
  • Solutions
  • Concanavalin A
  • Heparin
  • Adenine
  • Calcium