CD14brightCD16+ intermediate monocytes are induced by interleukin-10 and positively correlate with disease activity in rheumatoid arthritis
© The Author(s). 2017
Received: 5 September 2016
Accepted: 30 December 2016
Published: 10 February 2017
Three different subsets of circulating human monocytes, CD14brightCD16- (classical), CD14brightCD16+ (intermediate), and CD14dimCD16+ (non-classical) have been recently identified. It has been reported that CD14brightCD16+ monocytes are increased in rheumatoid arthritis (RA). However, the role of each monocyte subset in the pathogenesis of RA is still unclear. The purpose of this study was to investigate the association of CD14brightCD16+ monocytes with RA.
The study enrolled 35 patients with RA and 14 healthy volunteers. The three subsets of peripheral blood monocytes were analyzed by flow cytometry. Serum cytokines were measured at baseline in patients with RA and in healthy volunteers. CD14brightCD16- monocytes were isolated and cultured in vitro with different cytokines for 14 hours, and CD16 induction was assessed.
The proportion of CD14brightCD16+ monocytes, and serum interleukin (IL)-6, IL-8, and IL-10 were increased in patients with RA compared to healthy controls. The proportion of CD14brightCD16+ monocytes correlated with the disease activity of RA positively, whereas the proportion of CD14brightCD16- monocytes correlated negatively. When isolated CD14brightCD16- monocytes were stimulated with IL-6, IL-8, and IL-10, the only cytokine that significantly induced CD16 expression on the cells was IL-10.
The proportion of CD16brightCD14+ monocytes was positively correlated with RA disease activity. The expression of CD16 in monocytes was induced by IL-10 but not IL-6, and IL-8 was enhanced in the sera of patients with RA. Our results suggest that CD16brightCD14+ monocytes are involved in the pathogenesis of RA and that IL-10 is a key cytokine that regulates CD16 expression in monocytes.
KeywordsRheumatoid Arthritis Monocytes Interleukin-10 CD16
Rheumatoid arthritis (RA) is a systemic, autoimmune, and chronic inflammatory disease which causes pain and dysfunction and leads to the destruction of joints . The major inflammatory tissue is the synovium, the thin tissue that lines the joint. Immune cells, such as neutrophils, lymphocytes, and monocytes, produce inflammatory cytokines including interleukin (IL)-1, tumor necrosis factor-α (TNF-α), IL-6, and granulocyte-macrophage colony-stimulating factor (GM-CSF) , and are involved in the development of inflammation. It is well-known that peripheral blood monocytes are derived from precursors in the bone marrow, migrate into synovial tissue, and differentiate into macrophages that produce pro-inflammatory cytokines . Macrophages involved in synovial inflammation transform into osteoclasts, which cause joint destruction in RA [2, 4]. Osteoclasts are also derived from CD14+ monocytes under the influence of pro-inflammatory cytokines . Circulating CD14+ monocytes serve as precursors of endothelial cells and contribute to the process of angiogenesis in the tissue . Based on this background, the identification and classification of peripheral monocytes responsible for the disease is indispensable to understanding the pathogenesis of RA.
CD16 is a receptor for immunoglobulin (Ig) gamma Fc region III (FcγRIII). Fcγ receptors (FcγRs) are expressed on most of the cells involved in the immune system, including circulating monocytes, and they regulate immune responses through interaction with antibodies . According to these previous studies, immune complexes formed by anti-cyclic citrullinated peptide antibody (ACPA) and citrullinated peptide seem to bind to FcγRs and stimulate immune cell activation and release of inflammatory cytokines in patients with RA . Therefore, FcγRIII is one of the molecules possibly associated with the pathogenesis of RA. It has been reported that aberrant expression of FcγRIII, or the presence of allelic variants, can contribute to the pathogenesis of RA . However, the regulatory mechanisms of FcγRIII in RA are not fully understood.
Until now, circulating human monocytes have been classified into CD14+ CD16- (classical) and CD14+ CD16+ subsets according to their expression levels of CD14 and CD16 [10, 11]. It had been reported that CD14+ CD16+ monocytes are increased in patients with RA . Recently, a new third monocyte subpopulation, CD14brightCD16+ monocytes, was defined. According to the new classification system, the CD14+ CD16+ population is classified into CD14brightCD16+ (intermediate) and CD14dimCD16+ (non-classical) monocytes, depending on the level of CD14 expression . The CD14brightCD16- (classical) monocyte is the major subset, while the CD14brightCD16+ and CD14dimCD16+ subsets occur in lower numbers than classical monocytes .
It has been shown that the CD14brightCD16+ monocyte population increases in inflammatory or infectious conditions and, upon lipopolysaccharide stimulation [14, 15], produces TNF-α, IL-1β, IL-6, and IL-10. This newly classified CD14brightCD16+ monocyte population has been reported to be increased in patients with RA, whereas the CD14dimCD16+ monocyte population is not increased . It has been suggested that CD14brightCD16+ monocytes may migrate into the synovium from peripheral blood and differentiate into M1 or M2 macrophages in the tissue . However, the role of each subset in RA has not been fully clarified.
In this study, we sought to investigate the involvement of CD14brightCD16+ monocytes in the pathogenesis of RA, and possible mechanisms of the enhanced expression of CD16 on monocytes in patients with RA.
Subjects and study design
Patients with RA (n = 35) (mean age ± SD 59.8 ± 12.6 years, 82.9% female) who met the 2010 American College of Rheumatology/European League Against Rheumatism Classification criteria, and 14 healthy volunteers (mean age 49.2 ± 10.8 (range 30–72), 12 female) were enrolled into the study. All patients visited Keio University Hospital between January 2013 and May 2014 and had never been treated with methotrexate (MTX) or biological agents. They were considered to have moderate or high disease activity (scoring ≥3.2 on the 28-joint disease activity score based on erythrocyte sedimentation rate (DAS28-ESR). All participants gave written informed consent in accordance with the Declaration of Helsinki. MTX was initiated at an oral dose of 4–16 mg weekly. Monocyte subsets from peripheral blood samples were taken at baseline and after 12 weeks of MTX treatment in the patients. Clinical parameters including C-reactive protein (CRP), ESR, matrix metalloproteinase-3 (MMP-3), ACPA, and rheumatoid factor (RF) titers were obtained by routine clinical laboratory methods. DAS28-ESR scores, DAS28-CRP score, clinical disease activity index (CDAI), and simplified disease activity index (SDAI) were also determined at baseline and after 12 weeks of MTX treatment. Clinical characteristics of the patients were retrospectively collected from their medical records.
Monocyte subset determination
Heparinized whole blood was stained with phycoerythrin-Cy7 (PE-Cy7)-conjugated anti-CD14 (clone M5E2, BD Pharmingen, San Diego, CA, USA) and V450-conjugated anti-CD16 antibodies (clone 3G8, BD Horizon, San Jose, CA, USA), and analyzed using a flow cytometer with built-in software (MACSQuant Analyzer® and MACSQuantify® software, Miltenyi Biotec, Bergisch Gladbach, Germany). Monocyte subsets were identified on the basis of forward scatter/side scatter characteristics and CD14-positive gating. Subpopulations of CD14brightCD16-, CD14brightCD16+, and CD14dimCD16+ monocytes were distinguished by their surface expression pattern of CD14 and CD16 according to a previous report  and the proportion of each monocyte subset was determined.
Serum samples were collected at baseline and stored at -80 °C. Serum levels of GM-CSF, interferon-γ (IFN-γ), IL-1β, IL-10, IL-12p70, IL-2, IL-6, IL-8, and TNF-α were measured by multiplex electrochemiluminescence assay (Meso Scale Discovery SECTOR Imager 2400 platform®, Meso Scale Discovery, Rockville MD, USA). Serum macrophage colony-stimulating factor (M-CSF) levels were assessed by enzyme-linked immunosorbent assay (ELISA) (Quantikine® ELISA, Human M-CSF Immunoassay, R&D Systems Inc., Minneapolis MN, USA) and calculated using the manufacturer’s software. Values are expressed in pg/mL and presented as median with interquartile range (IQR).
Stimulation of peripheral monocytes in vitro
Peripheral blood mononuclear cells (PBMCs) were isolated from five healthy volunteers by density gradient centrifugation (Ficoll-Paque®, GE Healthcare, Uppsala, Sweden). To isolate monocyte subsets, cells were stained with phycoerythrin (PE)-conjugated anti-CD14 (clone MφP9, BD Pharmingen) and BV421-conjugated anti-CD16 antibodies (clone 3G8, BD Horizon) and sorted according to their CD14/CD16 expression using a cell sorter (BD Aria III®, BD Biosciences, San Jose CA, USA). CD14brightCD16- monocytes were cultured at 2.5 × 105/500 μL in Roswell Park Memorial Institute medium (RPMI-1640®, ATCC, Manassas, VA, USA) with 10% heat-inactivated fetal bovine serum (MP Biomedicals, Santa Ana CA, USA). They were then stimulated for 14 hours with either 100 ng/mL M-CSF, 1-100 (1, 10, 25, 50, or 100) ng/mL IL-10, 100 ng/mL IL-6, or 20 ng/mL IL-8 at 37 °C in a humidified atmosphere containing 5% CO2. The stimulated monocytes were stained with PE-conjugated anti-CD14, BV421-conjugated anti-CD16, and allophycocyanin (APC)-conjugated anti-HLA (human leukocyte antigen)-DR (clone LN3, eBioscience, San Diego CA, USA) antibodies and we analyzed the proportion of CD16+ monocytes using a flow cytometer.
Detection of IL-10 receptor expression
Heparinized whole blood cells from four healthy volunteers were stained with PE-Cy7-conjugated anti-CD14 (clone M5E2, BD Pharmingen), V450-conjugated anti-CD16 (clone 3G8, BD Horizon), and APC-conjugated anti-IL-10 receptor antibodies (clone 3F9, Biolegend, San Diego CA, USA), and the expression levels of IL-10 receptor on the CD14brightCD16- monocyte subset was evaluated.
IL-10 neutralization assay
CD14brightCD16- monocytes (2.5 × 105/500 μL) from the peripheral blood of four healthy volunteers were incubated with 25 ng/mL IL-10. In some experiments, anti-IL-10 receptor antibody (5 μg/mL) (clone 3F9, Biolegend) or rat IgG2aκ (5 μg/mL) to an irrelevant antigen (clone RTK2758, Biolegend) was added to the cultures. CD16 expression on monocytes was then measured.
We used commercial statistical software (JMP 11 system®, SAS Institute Inc., Cary NC, USA). The Wilcoxon rank sum test was used to assess the statistical significance of differences between groups. Correlation between two continuous variables was analyzed using Spearman’s rank correlation coefficient. Dunn’s test was used for multiple comparison procedures. A p value <0.05 was considered statistically significant.
Clinical characteristics of the patients with RA
Baseline characteristics of patients with rheumatoid arthritis at baseline
Total (n = 35)
Mean age, years
59.80 ± 12.64
Female, n (%)
Disease duration, months
41.9 ± 76.2
0.64 ± 0.59
35.7 ± 20.0
4.83 ± 0.91
4.02 ± 0.90
100.3 ± 84.8
RF-positive, n (%)
ACPA-positive, n (%)
18.99 ± 9.22
18.35 ± 9.03
0.85 ± 0.68
Changes in disease activity and the proportion of monocyte subsets in patients with rheumatoid arthritis (n = 35) at baseline and following 12 weeks of methotrexate treatment
Disease activity parameters
4.83 ± 0.91
3.53 ± 1.25
18.99 ± 9.87
10.24 ± 7.77
18.35 ± 9.03
9.84 ± 7.55
35.7 ± 20.0
27.2 ± 23.4
0.64 ± 0.59
0.35 ± 0.59
CD14brightCD16- monocytes (%)
72.16 ± 9.87
77.57 ± 9.36
CD14brightCD16+ monocytes (%)
13.96 ± 7.02
10.89 ± 7.25
CD14dimCD16+ monocytes (%)
8.14 ± 4.84
6.41 ± 4.20
Proportions of each monocyte subset
After 12 weeks of MTX treatment, the proportion of the CD14brightCD16+ population had significantly decreased from 14.0% to 10.9% and that of CD14brightCD16- monocytes had significantly increased from 72.2% to 77.6% in the patients with RA, while there was no significant difference in the proportion of CD14dimCD16+ monocytes between baseline and 12 weeks (Table 2).
Association between clinical parameters and monocyte subsets
Association between each monocyte subset and serum cytokine concentration
Serum levels of inflammatory cytokines at baseline in patients with rheumatoid arthritis (RA) and healthy volunteers
RA (n = 35)
HV (n = 14)
IL-10 induces surface CD16 expression on monocytes in vitro
In this study, we demonstrate that circulating CD14brightCD16+ monocytes are increased in patients with RA in the active phase and decrease after MTX treatment in a manner that correlates with decreasing disease activity. Moreover, this monocyte subset is associated with expression of inflammatory cytokines in peripheral blood, and the cytokine IL-10, which is increased in patients with RA, induces CD16 expression on monocytes. These results suggest that CD14brightCD16+ monocytes play a role in the pathogenesis of RA, and that IL-10 is a key cytokine in the regulation of CD16 expression.
Although an increase in CD14brightCD16+ monocytes in patients with RA has been reported , the possibility of correlation between CD14brightCD16+ monocytes and cytokines in untreated patients with active RA has not yet been investigated. Previous studies have not ruled out any influence of treatment on cytokine and disease activity, because the patients with RA in these studies were not treatment-naïve. Our results support previous observations  and show that the proportion of CD14brightCD16+ monocytes is increased in treatment-naïve patients with active RA compared to healthy controls, and is positively correlated with disease activity in these patients.
We further showed that the CD14brightCD16- population was negatively correlated with RA disease activity. Notably, the proportion of CD14brightCD16+ monocytes decreased and that of CD14brightCD16- monocytes increased when the patients received MTX treatment.
Though the function of CD14brightCD16+ monocytes in RA is not still clarified, this population may be involved in the pathogenesis of RA in accordance with our findings that CD14brightCD16+ monocytes decreased after MTX treatment. It has been shown that MTX inhibits inflammatory cytokine production  and cell proliferation in vitro, and to induce apoptosis of immune cells , but it has not been found to inhibit a specific subset of monocytes. One of the reasons for the decreased proportion of CD14brightCD16+ monocytes after MTX treatment was probably secondary to a phenomenon derived from the improvement in RA disease activity.
It is reported that M-CSF plays an important role in the introduction of CD14brightCD16+ monocytes. Anti-M-CSF antibody caused a decrease in circulating CD14brightCD16+ and CD14dimCD16+ monocytes in a clinical trial in two patients with active RA . Moreover, M-CSF and IFN-γ therapy has been found to induce CD16 expression on circulating monocytes in patients with cancer or lymphoma . CD16 expression has been shown to be induced in monocytes with culture of whole PBMCs with M-CSF or IL-10 on CD14brightCD16- monocytes in vitro . Although this report may indicate a possible direct role for cytokines, it did not exclude interactions with other cell subsets among the PBMCs. In our study, using highly purified CD14brightCD16- monocytes, we clearly showed that IL-10, but not M-CSF, directly induces CD16 expression in CD14brightCD16- monocytes. In addition, we proved that the enhancement of CD16 expression on CD14brightCD16- monocytes required the interaction with IL-10 and IL-10 receptor by a neutralization assay with anti-IL-10 receptor antibody.
It is well-known that IL-10 plays a crucial role, such as anti-inflammatory and/or pro-inflammatory roles in the pathogenesis of RA. IL-10 has been shown to inhibit production of IL-6, TNF-α, and GM-CSF from immune cells , and to enhance B cell differentiation to cells secreting IgG, IgM, and IgA [23, 24], resulting in increased RF and IgG-RF production by B cells in peripheral blood. Moreover, IL-10 is localized to the synovial membrane lining layer, the site of monocyte migration, and inhibits pro-inflammatory cytokines in RA . In this study, we demonstrated that serum IL-10 in patients with RA was significantly elevated compared with healthy volunteers, and was correlated with disease activity.
IL-10 is secreted by many kinds of cells such as T-cells, B-cells, macrophages, dendritic cells, natural killer cells, and monocytes themselves [26–28]. It is reported that CD16 expression on monocytes is maintained by IL-10 production by human naïve CD4+ T cells . The function of CD14brightCD16+ monocytes may be regulated by these cells producing IL-10. IL-10 tended to decrease in patients with RA with decreasing CD14brightCD16+ monocytes after 12 weeks of treatment. IL-10 may play a role in the induction of CD16 on monocytes in patients with RA.
We note two limitations to our study. First, the number of patients was relatively small, albeit large enough to provide statistically significant data. Second, we did not show that CD14brightCD16+ monocytes are directly associated with inflammatory cytokines in RA in vivo. Production of IL-6 and TNF-α in CD14brightCD16+ monocytes was not higher than that in CD14brightCD16-monocytes (Additional file 1). We thought that CD14brightCD16+ monocytes could exert both inflammatory and anti-inflammatory effects, and which effect’s dominance would depend on cells producing IL-10. The functions of these monocytes in RA will need to be clarified in future studies.
In conclusion, we have shown that CD14brightCD16+ monocyte proportions correlate with disease activity in patients with RA, and that CD16brightCD14+ monocytes are induced by IL-10 but not by other cytokines upregulated in serum from patients with RA. Our results suggest that CD16brightCD14+ monocytes are possibly involved in the pathogenesis of RA and that IL-10 should be a key cytokine that regulates CD16 expression in monocytes.
anti-cyclic citrullinated peptide antibody
clinical disease activity index
disease activity score in 28-joint count
enzyme-linked immunosorbent assay
erythrocyte sedimentation rate
receptor for immunoglobulin gamma Fc region III
granulocyte-macrophage colony-stimulating factor
health assessment questionnaire
human leukocyte antigen
macrophage colony-stimulating factor
mean fluorescence intensity
simplified disease activity index
tumor necrosis factor
The authors sincerely thank Ms Harumi Kondo and Ms Mayumi Ota for helping with the acquisition of clinical information.
This work was supported by an institutional research grant from Keio University.
Availability of data and materials
Supplemental Method and Figure.
MT, NS, KYo, KS, Kya, and TT were involved in drafting the manuscript. All authors were involved in revising it critically for important intellectual content, and revising the final version. TT had full access to all data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. All authors participated in the study conception and design and participated in the acquisition of data, and analysis and interpretation of data. All authors read and approved the manuscript.
MT and KYo have conflicts of interest to declare. NS has received research grants from Chugai Pharmaceutical Co., Ltd., Mitsubishi Tanabe Pharma Co., Ono Pharmaceutical Co., Ltd. and Nippon Kayaku Co., Ltd. KS has received research grants from Eisai Co., Ltd., and Bristol-Myers Squibb. KYa has received consultant fees from Pfizer, Chugai Pharmaceutical Co., Ltd, Mitsubishi-Tanabe Pharma Co., and Abbvie, and received honoraria from Pfizer, Chugai Pharmaceutical Co., Ltd, Mitsubishi-Tanabe Pharma Co., Bristol-Myers Squibb, Takeda Industrial Pharma, GlaxoSmithkline, Nippon Shinyaku, Eli lilly, Janssen Pharma, Eisai Pharma, Astellas Pharma, and Acterlion Pharmaceuticals and received research support from Chugai Pharma and Mitsubishi-Tanabe Pharma. TT has received lecture fees or research grants from Abbott Japan Co., Ltd., Astellas Pharma, Bristol-Myers K.K., Chugai Pharmaceutical Co, Ltd., Daiichi Sankyo Co., Ltd., Eisai Co., Ltd., Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Co., Pfizer Japan Inc., Sanofi-Aventis K.K., Santen Pharmaceutical Co., Ltd., Teijin Pharma Ltd., Asahikasei Pharma Corp., Taisho Toyama Pharmaceutical Co., Ltd., Janssen Pharmaceutical K.K., Astra Zeneca K.K., Eli Lilly Japan K.K., Novartis Pharma K.K., and Abbvie GK.
Consent for publication
Written informed consent was obtained from the patients for publication of their individual details in this article. The consent forms are held by the authors and are available for review by the Editor-in-Chief of this journal.
Ethics approval and consent to participate
This study was approved by the institutional review board of Keio University School of Medicine, and it was conducted in compliance with the Declaration of Helsinki. The participants gave informed consent to participate.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Feldmann M. Development of anti-TNF therapy for rheumatoid arthritis. Nat Rev Immunol. 2002;2:364–71.View ArticlePubMedGoogle Scholar
- McInnes IB, Schett G. The pathogenesis of rheumatoid arthritis. N Engl J Med. 2011;365:2205–19.View ArticlePubMedGoogle Scholar
- Shi C, Pamer EG. Monocyte recruitment during infection and inflammation. Nat Rev Immunol. 2011;11:762–74.View ArticlePubMedPubMed CentralGoogle Scholar
- Kennedy A, Fearon U, Veale DJ, et al. Macrophages in synovial inflammation. Front Immunol. 2011;2:52. doi:10.3389/fimmu.2011.00052.View ArticlePubMedPubMed CentralGoogle Scholar
- Massey HM, Flanagan AM. Human osteoclasts derive from CD14-positive monocytes. Br J Haematol. 1999;106:167–70.View ArticlePubMedGoogle Scholar
- Arras M, Ito WD, Scholz D, et al. Monocyte activation in angiogenesis and collateral growth in the rabbit hindlimb. J Clin Invest. 1998;101:40–50.View ArticlePubMedPubMed CentralGoogle Scholar
- Hogarth PM, Pietersz GA. Fc receptor-targeted therapies for the treatment of inflammation, cancer and beyond. Nat Rev Drug Discov. 2012;11:311–31.View ArticlePubMedGoogle Scholar
- Solomon S, Kassahn D, Illges H. The role of the complement and the Fc gamma R system in the pathogenesis of arthritis. Arthritis Res Ther. 2005;7:129–35.View ArticlePubMedPubMed CentralGoogle Scholar
- Takai T. Roles of Fc receptors in autoimmunity. Nat Rev Immunol. 2002;2:580–92.PubMedGoogle Scholar
- Passlick B, Flieger D, Ziegler-Heitbrock HW. Identification and characterization of a novel monocyte subpopulation in human peripheral blood. Blood. 1989;74:2527–34.PubMedGoogle Scholar
- Wong KL, Yeap WH, Tai JJ, et al. The three human monocyte subsets: implications for health and disease. Immunol Res. 2012;53:41–57.View ArticlePubMedGoogle Scholar
- Kawanaka N, Yamamura M, Aita T, et al. CD14+, CD16+ blood monocytes and joint inflammation in rheumatoid arthritis. Arthritis Rheum. 2002;46:2578–86.View ArticlePubMedGoogle Scholar
- Ziegler-Heitbrock L, Ancuta P, Crowe S, et al. Nomenclature of monocytes and dendritic cells in blood. Blood. 2010;116:e74–80.View ArticlePubMedGoogle Scholar
- Rossol M, Kraus S, Pierer M, et al. The CD14(bright) CD16+ monocyte subset is expanded in rheumatoid arthritis and promotes expansion of the Th17 cell population. Arthritis Rheum. 2012;64:671–7.View ArticlePubMedGoogle Scholar
- Skrzeczyńska-Moncznik J, Bzowska M, Loseke S, et al. Peripheral blood CD14high CD16+ monocytes are main producers of IL-10. Scand J Immunol. 2008;67:152–9.View ArticlePubMedGoogle Scholar
- Yang J, Zhang L, Yu C, et al. Monocyte and macrophage differentiation: circulation inflammatory monocyte as biomarker for inflammatory diseases. Biomark Res. 2014;2:1. doi:10.1186/2050-7771-2-1.View ArticlePubMedPubMed CentralGoogle Scholar
- Korkosz M, Bukowska-Strakova K, Sadis S, et al. Monoclonal antibodies against macrophage colony-stimulating factor diminish the number of circulating intermediate and nonclassical (CD14(++)CD16(+)/CD14(+)CD16(++)) monocytes in rheumatoid arthritis patients. Blood. 2012;119:5329–30.View ArticlePubMedGoogle Scholar
- Abeles RD, McPhail MJ, Sowter D, et al. CD14, CD16 and HLA-DR reliably identifies human monocytes and their subsets in the context of pathologically reduced HLA-DR expression by CD14(hi)/CD16(neg) monocytes: Expansion of CD14(hi)/CD16(pos) and contraction of CD14(lo)/CD16(pos) monocytes in acute liver failure. Cytometry A. 2012;81:823–34.View ArticlePubMedGoogle Scholar
- Chan ES, Cronstein BN. Molecular action of methotrexate in inflammatory diseases. Arthritis Res. 2002;4:266–73.View ArticlePubMedPubMed CentralGoogle Scholar
- Cutolo M, Sulli A, Pizzorni C, et al. Anti-inflammatory mechanisms of methotrexate in rheumatoid arthritis. Ann Rheum Dis. 2001;60:729–35.View ArticlePubMedPubMed CentralGoogle Scholar
- Weiner LM, Li W, Holmes M, et al. Phase I trial of recombinant macrophage colony-stimulating factor and recombinant gamma-interferon: toxicity, monocytosis, and clinical effects. Cancer Res. 1994;54:4084–90.PubMedGoogle Scholar
- Jinquan T, Larsen CG, Gesser B, et al. Human IL-10 is a chemoattractant for CD8+ T lymphocytes and an inhibitor of IL-8-induced CD4+ T lymphocyte migration. J Immunol. 1993;151:4545–51.PubMedGoogle Scholar
- O’Garra A, Chang R, Go N, et al. Ly-1 B (B-1) cells are the main source of B cell-derived interleukin 10. Eur J Immunol. 1992;22:711–7.View ArticlePubMedGoogle Scholar
- Rousset F, Garcia E, Defrance T, et al. Interleukin 10 is a potent growth and differentiation factor for activated human B lymphocytes. Proc Natl Acad Sci USA. 1992;89:1890–3.View ArticlePubMedPubMed CentralGoogle Scholar
- Katsikis PD, Chu CQ, Brennan FM, et al. Immunoregulatory role of interleukin 10 in rheumatoid arthritis. J Exp Med. 1994;179:1517–27.View ArticlePubMedGoogle Scholar
- Blanco E, Moñux G, Mas A, et al. Role of IL-10 promoter polymorphisms in the development of severe aorto-iliac occlusive disease. Hum Immunol. 2008;69:651–4.View ArticlePubMedGoogle Scholar
- Seki S, Osada S, Ono S, et al. Role of liver NK cells and peritoneal macrophages in gamma interferon and interleukin-10 production in experimental bacterial peritonitis in mice. Infect Immun. 1998;66:5286–94.PubMedPubMed CentralGoogle Scholar
- Chomarat P, Rissoan MC, Banchereau J, et al. Interferon gamma inhibits interleukin 10 production by monocytes. J Exp Med. 1993;177:523–7.View ArticlePubMedGoogle Scholar
- Liu Y, Yang B, Ma J, et al. Interleukin-21 maintains the expression of CD16 on monocytes via the production of IL-10 by human naïve CD4+ T cells. Cell Immunol. 2011;267:102–8.View ArticlePubMedGoogle Scholar