T. Hjort, QUANTITATIVE-DETERMINATION OF IGG AND IGA ON SPERM FROM INFERTILE PATIENTS WITH AND WITHOUT ANTISPERM ANTIBODIES, American journal of reproductive immunology [1989], 36(4), 1996, pp. 211-215
Immunoglobulins on patients sperm were determined by an ELISA techniqu
e, modified from the RIA described by Haas and D'Cruz (Am J Reprod Imm
unol, 1989; 20:37-43), i.e., suspensions of washed sperm (40, 20, 10,
and 5 mill/ml) were added to a dilution of peroxydase-labelled anti-Ig
G or anti-IgA, and after incubation the supernatants were transferred
to cups in microtrays, coated with IgG or IgA, respectively. After inc
ubation and washing ELISA reaction was carried out. Known amounts of I
gG and IgA were processed in the same way to obtain a standard curve,
allowing the Ig on the sperm to be expressed in ng/mill sperm. Ejacula
tes with increased viscosity revealed high values, irrespective of MAR
-results and in some cases the same was true for samples with large nu
mbers of non-spermatozoal cells (NSC). However, among 48 samples from
men from infertile couples with negative MAR, > 20 mill sperm/ml, norm
al viscosity, and a ratio between sperm and NSC > 5, the median for Ig
G was 0.2 ng/mill sperm, 90% had less than or equal to 0.8 ng/mill spe
rm, and the highest value recorded was 1.9 ng/mill sperm. For IgA the
median was 0.5 ng, 90% of the 47 samples contained less than or equal
to 1.9 ng, and the highest value was 3.1 ng/mill sperm. The values for
sperm from patients with a positive MAR, but without free antibodies
in seminal plasma, were generally within the normal range. In contrast
, increased values were recorded for most of the patients with free an
tibodies in seminal plasma, up to 4.2 ng/mill sperm for IgG and up to
12.5 ng/mill sperm for IgA.