Evaluation for antisperm antibodies after storage of sperm in TEST-yolk buffer.

Fertil Steril

Department of Obstetrics and Gynecology, University of Minnesota, Minneapolis 55455, USA.

Published: September 1996

AI Article Synopsis

  • The study aimed to evaluate if TEST-yolk buffer impacts the presence of antisperm antibodies on sperm by using immunobead tests conducted before and after incubation in the buffer.
  • Despite the 24-hour storage at 4°C, there were no significant changes in antibody presence, as most samples retained their initial antibody status, indicating TEST-yolk buffer effectively preserves sperm without altering antibody detection.
  • However, variability in indirect immunobead tests suggests potential changes in sperm antigens, meaning while the buffer is suitable for storage, it may slightly affect antigen composition.

Article Abstract

Objective: To determine if TEST-yolk buffer, consisting of TES (N-tris [hydroxymethyl]-methyl-2-aminoethanesufonic acid), Tris (Tris[hydroxymethyl]aninomethane), and chicken egg yolk, affects the presence of antisperm antibodies on the sperm surface as detected by the immunobead test.

Design: A prospective study of antisperm antibodies on sperm surface before and after incubation in TEST-yolk buffer. Direct immunobead test and indirect immunobead test were done the day of collection of the semen sample to detect the presence of human immunoglobulin class G (IgG) and immunoglobulin class A (IgA); immunobead tests were repeated on the same sperm samples after 24 hours of storage in TEST buffer.

Setting: Academic tertiary institution.

Participants: Patients undergoing evaluation for infertility.

Results: There was no significant difference in the outcome of the direct immunobead test after extending semen samples with TEST-yolk buffer for 24 hours at 4 degrees C. Eleven samples that were initially negative for IgG and 13 samples that were negative for IgA remained negative after 24-hour storage in TEST-yolk buffer. Eleven samples that were positive for IgG and nine samples that were positive for IgA by the direct immunobead test the first day remained positive the next day. Five extended sperm samples used in the indirect immunobead test with IgG positive serum gave positive results and four of five used with IgA positive serum gave positive results.

Conclusions: These findings suggest that TEST-yolk buffer can be used to extend semen without affecting the presence of antibodies on the sperm surface as indicated by the direct immunobead test. The higher variability of the indirect immunobead tests indicates there may be some alteration of sperm antigens after storing in TEST-yolk buffer. These findings indicate that TEST-yolk buffer can be used to store semen for batched processing of samples or as a transport medium for delivery to a central laboratory for antibody testing.

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Source
http://dx.doi.org/10.1016/s0015-0282(16)58518-5DOI Listing

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