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Lack of inhibition by mouse alpha-foetoprotein (AFP) of in vitro induced lymphocyte blastogenesis

Annales D'Immunologie
|February 1, 1978
PubMed

Insights

Mouse amniotic fluids (MAF) can suppress lymphocyte transformation, but purified mouse alpha-fetoprotein (AFP) does not show this immunosuppressive activity. This suggests other factors in MAF are responsible for the observed immune modulation.

Area of Science:

  • Immunology
  • Reproductive Biology
  • Biochemistry

Background:

  • Mouse amniotic fluids (MAF) have been anecdotally reported to possess immunosuppressive properties.
  • Lymphocyte transformation assays are standard methods for evaluating immune cell activation and response.

Purpose of the Study:

  • To investigate the immunosuppressive effects of MAF on lymphocyte transformation.
  • To determine if mouse alpha-fetoprotein (AFP) is responsible for the observed immunosuppressive activity in MAF.

Main Methods:

  • Lymphocyte transformation assays were performed using concanavalin A, phytohemagglutinin, and lipopolysaccharide.
  • Mixed lymphocyte cultures were utilized to assess immune cell interactions.
  • Purification of mouse alpha-fetoprotein (AFP) was achieved through immunoadsorption and affinity chromatography.
  • Oestrogen levels were manipulated by adding oestradiol-17 beta or removing endogenous oestrogens via dialysis.

Main Results:

  • Eight out of thirteen MAF samples exhibited significant inhibitory activity on lymphocyte transformation.
  • Purified mouse alpha-fetoprotein (AFP) showed no significant inhibitory effect on lymphocyte transformation, regardless of its origin from suppressive or non-suppressive MAF.
  • The observed suppressive properties of MAF and the lack of activity in purified AFP were not altered by oestradiol-17 beta or oestrogen removal.

Conclusions:

  • The immunosuppressive activity found in MAF is not attributable to mouse alpha-fetoprotein (AFP).
  • Other unidentified components within MAF likely mediate the observed immunosuppression.
  • Oestrogens do not appear to be the primary mediators of MAF's immunosuppressive effects in this context.

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