Abstract. The technique of counterimmunoelectrophoresis (CIE) has been used to detect precipitin reactions between sera from subfertile and fertile patients and seminal plasma antigens. Freshly ejaculated seminal plasma lacked antigenicity detectable by CIE. Seminal plasmas obtained as part of routine semen analyses and therefore left to stand for varying periods, showed activity. In a study of 60 spouse seminal plasmas which were collected in routine fashion and then incubated at 37°C, antigenic activity appeared after varying periods of incubation. Activity was most commonly detected after 18 hours' incubation usually lasting for 6 hours or more. A pool of 37 seminal plasmas (PSP), which was rendered antigenic by incubation, reacted on CIE with 156 (85.7%) of 182 sera from subfertile patients and with 80 (63.0%) of 127 sera from fertile women. In three of the positive sera, the immunoglobulin fraction was recovered and found to contain the components binding with PSP antigen. The PSP material was bacteriologically contaminated and on culture 7 bacterial types were isolated–pseudo‐monas aeruginosa, proteus mirabilis, bacillus subtilis, non‐haemolytic and haemolytic diphtheroids, mucoid E. coli, and streptococcus faecalis. Pooled cell free extracts (CFE) from these bacteria reacted with 154 (84.6%) of the subfertility patients and 68 (53.5 %) of the comparison subjects. Use of a 3‐well CIE procedure revealed the presence of some of these CFE bacterial antigens in PSP. A component distinct from the bacterial antigens was observed in PSP. This antigenic component is thought to represent seminal plasma antigen(s) resulting from bacterial action. Its appearance is induced by contact of seminal plasma with any of the 7 bacterial types, but not by incubation of sterile seminal plasma alone, or in combination with CFE or bacterial protease. A proportion of the bacterial antigen(s) was heat labile. Those that were thermostable were removed from PSP by absorption with chicken anti‐bacterial antisera. The absorbed PSP reacted with 58 (31.2%) of the subfertile subjects and 15 (11.8%) of the fertile women. The subfertile group was subdivided into primary and secondary subfertility, and again according to whether conception occurred during the course of the study. A difference in CIE positivity was observed in the secondary, but not in the primary, subfertile women. Twenty‐two (61.1 %) of the 36 secondary subfertile women who failed to conceive were CIE positive, in contrast to 6 (20.7%) of the 29 women who became pregnant (p<0.005).
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