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. Author manuscript; available in PMC: 2012 Nov 15.
Published in final edited form as: Pathol Res Pract. 2011 Oct 13;207(11):680–685. doi: 10.1016/j.prp.2011.08.007

Fig. 3.

Fig. 3

Flow cytometric analysis of endometrial biopsies represents a powerful approach for identification of upper genital tract leukocytes (representative contour plots shown). After defining the CD45+ cell population (not shown), a large percentage was identified as (A) CD11b+, and (B, C) further identified as macrophages (CD11int/hiCD14+CD68+) (B, D) neutrophils (CD11bhiCD14-CD15+), and (B) another myeloid cell subpopulation (CD11bloCD14CD11). (E) To characterize T cell populations, CD11b cells were interrogated for CD3 expression. Both CD4+ and CD8+ cell populations were clearly defined (F), allowing exploration of their functional activation status, as indicated by the levels of CD69 (G) and granzyme B (H) expression. For plasma cell identification, CD3 and CD11b cells were interrogated for CD19 (J) and CD138 (K) expression. All CD138+ cells were CD27+ while a significant portion were CD38+ (L), strong evidence for the proper identification of a plasma cell population.