Interactions of the conceptus with the immune system can involve eithe
r anti-sperm or anti-conceptus immune responses that limit the success
of pregnancy or beneficial effects of cytokines released from lymphoi
d cells on embryonic growth and gene expression. The immune system is
functional in the uterus and therefore there is the potential for anti
-conceptus immune responses. However, endometrial lymphocytes are dist
inct in many respects from lymphoid cells at peripheral sites; one maj
or subpopulation expresses the gamma delta T-cell receptor and may not
recognize major histocompatibility antigens. There are also several c
ontrol systems to limit anti-conceptus immune responses. In particular
, expression of major histocompatibility antigens on the trophoblast i
s either absent or of limited distribution. In addition, activation of
anti-conceptus immune responses leading to cytolytic responses is fur
ther limited by the presence of molecules that can inhibit lymphocyte
transformation. The most well-characterized of these are prostaglandin
E(2) from placental and endometrial tissues, interferon-tau from the
trophoblast during early pregnancy, and two endometrial proteins calle
d the uterine milk proteins (UTMP). Progesterone plays a central role
in inhibition of immune responses in actions that are mediated at leas
t in part through endometrial secretion of UTMP. Cytokines play import
ant roles as autocrine and paracrine regulators in many tissues includ
ing the reproductive tract. In ruminants, the best described example i
s interferon-tau. Other cytokines found in the reproductive tract or p
roduced by the conceptus include interleukin-1, leukaemia inhibitory f
actor, granulocyte-macrophage colony stimulating factor and interleuki
n-6. It is possible that the major source of cytokines in the reproduc
tive tract is non-lymphoid cells of the endometrium and trophoblast. I
t is not known to what extent endometrial lymphocytes contribute to th
e cytokine milieu because no cytokine has been identified as a product
of endometrial lymphocytes. However, there is a population of granula
ted lymphocytes that increase in number and granularity in the luminal
epithelium of the late-pregnant ewe that is a potential source of cyt
okines.