Hepatic leukocytes were recovered as described previously. 9 Cells were analyzed by flow cytometry, were cultured for cytokine determination, or were centrifuged onto glass slides with a Shandon Cytospin 2 (Thermo Fisher Scientific, Waltham, MA) for differential cell counting

(300 cells per sample counted). Cells were restimulated ex vivo, stained, and analyzed as described. 9, 12 The employed antibodies were specific for CD4 (clone RM4-5), CD62L (clone MEL-14), CD11b (clone M1/70), chemokine (C-C motif) receptor 9 (CCR9; clone CD-1.2; eBioscience, San Diego, CA), α4β7 (clone DATK32), lymphocyte antigen 6 complex locus G (Ly6-G; clone 1A8), IL-4 (clone 11B11; BD Pharmingen, San Jose, CA), and F4/80 (clone BM8; Caltag, Carlsbad, CA).

Appropriate Erlotinib purchase isotype-matched clones served as controls and were used to set analysis gates. Hepatic leukocytes were restimulated in vitro with medium or somatic larval antigens at 10 μg per well. After 3 days, supernatants were collected, and IL-4 levels were determined by enzyme-linked immunosorbent assay as described. 9 ALT activity was measured in individual serum samples with a commercially available kit from Pointe Scientific (Canton, MI). Liver tissue was fixed in 10% neutral-buffered formalin and embedded in paraffin. Six-micrometer sections were stained with hematoxylin and eosin for microscopic examination. Photomicrographs were created with a BX51 microscope and a DP12 digital camera system from Olympus (Center Valley, PA). Mesenteric lymph nodes from WT mice were obtained 5 days after oral infection. CD4+ T cells were purified by negative selection with the CD4+ T cell isolation 3MA kit from Miltenyi Biotec (Auburn, CA). The percentage of CD4+ cells was determined to be ≥95% by flow cytometry. Cells (2 × 106) in 0.5 mL of phosphate-buffered saline (PBS) or PBS alone were injected intraperitoneally into IL-10 KO recipients 1 day prior to their infection.

In some groups of recipients, a control IgG or α-IL-10R (clone 1B1.3a) antibody (300 μg intraperitoneally every other day beginning 1 day before infection) was administered. Other groups included mice that were given cells and PBS or PBS only. To aid in the interpretation of the effects of the α-IL-10R treatment, we also included a group MCE公司 of WT recipients that were given the same dose and regimen as the IL-10 KO mice. Twelve days later, mice were evaluated for ALT activity, liver histology, hepatic leukocyte content (total, CD4+α4β7+ cells, and Ly6-G+F4/80− cells), and cytokine production. Each experiment was performed three to five times, and each group contained three to five mice. Means and standard deviations were calculated from values obtained from individual mice in a treatment group. Means were compared by the Student t test or analysis of variance followed by an appropriate posttest with GraphPad Prism software (San Diego, CA). Significance was assessed at P < 0.05.