Sperm Phagocytosis by Human Peritoneal Macrophages

In: Obstetrical & Gynecological Survey · 1983 · vol. 38(3) , pp. 177–178 · doi:10.1097/00006254-198303000-00022 · W2053125754
article OA: closed CC0 ⤵ 4 in-corpus citations
Full text JSON View on OpenAlex View at publisher
AI-generated summary by gemini-2.5-flash-lite, 2026-06-10

Peritoneal macrophages from infertile women with endometriosis exhibited higher sperm phagocytosis in vitro compared to those from infertile women without endometriosis.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by qwen3.7-flash, 2026-08-30 · read from full text

This study investigated the role of peritoneal macrophages in infertility by comparing sperm phagocytosis rates among fertile women, infertile women without endometriosis, and infertile women with endometriosis. The researchers found that macrophage counts were significantly higher in infertile groups, particularly in those with endometriosis, and these cells exhibited a greater capacity to phagocytose sperm compared to controls. These findings suggest that the increased presence and activity of peritoneal macrophages in endometriosis patients may directly contribute to infertility by impairing gamete function. This paper is centrally about endometriosis — specifically exploring how peritoneal immune responses associated with the condition may cause infertility through sperm destruction.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

Pelvic endometriosis is associated with infertility even in women with few peritoneal implants, who ovulate, and have anatomically patent oviducts. Since peritoneal fluid is in contact with peritoneal endometrial implants as well as with the microenvironment in which fertilization occurs, it has the potential to influence fertilization adversely. The volume of peritoneal fluid in women of reproductive age varies with the menstrual cycle and is increased in women with endometriosis. This fluid contains variable numbers of leukocytes, of which more than 85 per cent are mononuclear phagocytes (macrophages). Because peritoneal macrophages have access to the reproductive tract via the oviducts, the authors of the present report conjectured that these cells might inhibit fertilization by injuring gametes. Women in the study were divided into three groups: (I) multiparous women (N = 10) who underwent laparoscopic tubal cauterization for sterilization or tubal rean-astomosis for reversal of previous sterilization; (II) infertile women (N = 12) without endometriosis; and (III) infertile women (N = 10) with endometriosis, who underwent diagnostic laparoscopy or therapeutic laparotomy. Peritoneal fluid from these patients was subjected to a sperm phagocytosis assay in vitro. The peritoneal fluid cells from all patients were predominantly macrophages, with few lymphocytes and only rare polymorphonuclear leukocytes. The cells displayed abundant cytoplasm, numerous lysosomes, phagocytic capability for antibody opsonized erythrocytes and latex particles, and nonspecific esterase positivity. Morphologically, macrophages from patients of the different groups did not appear to be different in size, vacuolization, or staining characteristics. Fertile patients (group I) had fewer total peritoneal macrophages (2.6 ± 0.7 × 106; mean ± SE) than did infertile patients without endometriosis (group II) (8.1 ± 2.7 × 106; P < 0.002) or infertile patients with endometriosis (group III) (18.2 ± 4.2 × 106; P < 0.002). Macrophages from group III were significantly more numerous than those from group II (P < 0.02). The phagocytosis assay actually measures both macrophage sperm phagocytosis and adherence to the mac-rophage surface. By light and transmission electron microscopy, the bulk was observed to be phagocytosis and not adherence to macrophages. No nonspecific adherence of sperm to the plastic was noted in control sperm chambers with macrophages and sperm. Macrophages from infertile patients with endometriosis (group III) had higher sperm phagocytosis than did those from infertile women without endometriosis in group II (primarily women with adnexal adhesions and tubal obstruction) (P < 0.002).
Full text 2,869 characters · extracted from oa-doi-fallback · click to expand
Sperm Phagocytosis by Human Peritoneal Macrophages A Possible Cause of Infertility in Endometriosis - JOSEPH J. MUSCATO - A. F. HANEY - J. BRICE WEINBERG Pelvic endometriosis is associated with infertility even in women with few peritoneal implants, who ovulate, and have anatomically patent oviducts. Since peritoneal fluid is in contact with peritoneal endometrial implants as well as with the microenvironment in which fertilization occurs, it has the potential to influence fertilization adversely. The volume of peritoneal fluid in women of reproductive age varies with the menstrual cycle and is increased in women with endometriosis. This fluid contains variable numbers of leukocytes, of which more than 85 per cent are mononuclear phagocytes (macrophages). Because peritoneal macrophages have access to the reproductive tract via the oviducts, the authors of the present report conjectured that these cells might inhibit fertilization by injuring gametes. Women in the study were divided into three groups: (I) multiparous women (N = 10) who underwent laparoscopic tubal cauterization for sterilization or tubal rean-astomosis for reversal of previous sterilization; (II) infertile women (N = 12) without endometriosis; and (III) infertile women (N = 10) with endometriosis, who underwent diagnostic laparoscopy or therapeutic laparotomy. Peritoneal fluid from these patients was subjected to a sperm phagocytosis assay in vitro. The peritoneal fluid cells from all patients were predominantly macrophages, with few lymphocytes and only rare polymorphonuclear leukocytes. The cells displayed abundant cytoplasm, numerous lysosomes, phagocytic capability for antibody opsonized erythrocytes and latex particles, and nonspecific esterase positivity. Morphologically, macrophages from patients of the different groups did not appear to be different in size, vacuolization, or staining characteristics. Fertile patients (group I) had fewer total peritoneal macrophages (2.6 ± 0.7 × 106; mean ± SE) than did infertile patients without endometriosis (group II) (8.1 ± 2.7 × 106; P < 0.002) or infertile patients with endometriosis (group III) (18.2 ± 4.2 × 106; P < 0.002). Macrophages from group III were significantly more numerous than those from group II (P < 0.02). The phagocytosis assay actually measures both macrophage sperm phagocytosis and adherence to the mac-rophage surface. By light and transmission electron microscopy, the bulk was observed to be phagocytosis and not adherence to macrophages. No nonspecific adherence of sperm to the plastic was noted in control sperm chambers with macrophages and sperm. Macrophages from infertile patients with endometriosis (group III) had higher sperm phagocytosis than did those from infertile women without endometriosis in group II (primarily women with adnexal adhesions and tubal obstruction) (P < 0.002).

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

endometriosisinfertility

Citation neighborhood (sparse)

Too few in-corpus citations on either side for a chart; here are the lists.

Cited by (4)

Cited by (4)

Source provenance

openalex
last seen: 2026-06-10T17:14:06.276822+00:00
unpaywall
last seen: 2026-09-21T07:16:15.697306+00:00
License: CC0 · commercial use OK