Changes in peripheral blood inflammatory factors (TNF-α and IL-6) and intestinal flora in AIDS and HIV-positive individuals

Changes in peripheral blood inflammatory factors (TNF-α and IL-6) and intestinal flora in AIDS and HIV-positive individuals AIDS和HIV阳性个体外周血炎症因子(TNF-α和IL-6)和肠道菌群的变化研究 first-author corresp ‡Corresponding Author ‡Corresponding Author †E-mail:duanjianping20@163.com †E-mail:duanjianping20@163.com duanjianping20@163.com Department of Infectious Disease, Qingdao Sixth People’s Hospital, Qingdao 266033, China Department of Infectious Disease, Qingdao Sixth People’s Hospital, Qingdao 266033, China Objective: 2 In this study, we investigated the changes in peripheral blood inflammatory factors and intestinal flora in acquired immune deficiency syndrome (AIDS) and human immunodeficiency virus (HIV)-positive individuals (AIDS/HIV patients), and explored the relationships among intestinal flora, peripheral blood inflammatory factors, and CD4 + T lymphocytes. Methods: 2 Thirty blood and stool samples from an AIDS group and a control group were collected. The levels of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) were determined by enzyme-linked immunosorbent assay (ELISA), and the number of CD4 + T lymphocytes by a FACSCount automated instrument. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to determine the messenger RNA (mRNA) levels of Bifidobacterium , Lactobacillus , Escherichia coli , Enterococcus faecalis , and Enterococcus faecium . Correlations among intestinal flora, inflammatory factor levels, and CD4 + T lymphocyte values were evaluated using the Spearman correlation coefficient. Results: 2 The levels of TNF-α and IL-6 in the AIDS group were higher than those in the control group, while the number of CD4 + T lymphocytes was lower. The amounts of Bifidobacterium and Lactobacillus in the AIDS group were significantly lower than those in control group, while the amounts of E . coli , E . faecalis , and E . faecium were much higher. The amounts of Bifidobacterium and Lactobacillus were negatively correlated with the content of TNF-α and IL-6 and the CD4 + T lymphocyte count, while those correlations were reversed for E . coli , E . faecalis , and E . faecium . Conclusions: 2 The intestinal microbiota of AIDS/HIV patients were disordered, and there was a correlation between the amount of intestinal flora and the number of CD4 + T lymphocytes and the levels of TNF-α and IL-6. 目的 2 本研究探究获得性免疫缺陷综合征(AIDS)和人类免疫缺陷病毒(HIV)阳性个体患者外周血炎症因子和肠道菌群的变化,同时探讨了肠道菌群、外周血炎症因子和CD4 + T淋巴细胞之间的关系. 创新点 2 首次探讨了AIDS和HIV阳性个体患者中肠道菌群、外周血炎症因子和CD4 + T淋巴细胞之间的关系. 方法 2 从艾滋病组和对照组分别收集30份血液和粪便样本.使用酶联免疫吸附测定(ELISA)法测定肿瘤坏死因子(TNF-α)和白细胞介素-6(IL-6)的水平;用流式细胞仪测定CD4 + T淋巴细胞数目;采用实时定量聚合酶链式反应(qRT-PCR)法检测双歧杆菌、乳酸菌、大肠杆菌、粪肠球菌和屎肠球菌的mRNA水平;采用Spearman分析肠道菌群、炎症因子与CD4 + T淋巴细胞之间的相关性. 结论 2 不但AIDS/HIV患者体内肠道菌群紊乱,而且肠道菌群数量与CD4 + T淋巴细胞数量以及TNF-α、IL-6水平存在相关性. Acquired immune deficiency syndrome (AIDS) Tumor necrosis factor-α(TNF-α) Interleukin-6 (IL-6) Intestinal flora CD4 + T lymphocytes 获得性免疫缺陷综合征 肿瘤坏死因子(TNF-α) 白细胞介素-6(IL-6) 肠道菌群 CD4 + T淋巴细胞 Introduction 1 Acquired immune deficiency syndrome (AIDS) is an immune system disease caused by human immunodeficiency virus (HIV) infection and CD4 + T cell depletion. AIDS patients have several co-morbidities, including gastrointestinal disease, systemic immune activation, malignancy, liver disease, bone disease, and neurological complications (Capeau, 2011 2011 ; Kolgiri and Patil, 2017 2017 ), which have a clear impact on survival. Previous studies have reported that antiretroviral therapy (ART) successfully controls systemic HIV replication, but immune recovery is variable (Maartens et al., 2014 2014 ; Monaco et al., 2016 2016 ). One of the characteristics of AIDS is a rapid depletion of CD4 + T cells in the gut-associated lymphoid tissue (Klatt et al., 2008 2008 ). In addition, AIDS can lead to gastrointestinal disease characterized by increased gastrointestinal inflammation, diarrhea, and malabsorption (Brenchley, 2013 2013 ). It has been reported that dysbiosis of the microbiota plays an important role in gut dysfunction and gastrointestinal inflammation (Klase et al., 2015 2015 ). The human intestine is a complex ecosystem inhabited by the microbiome, including bacteria, viruses, archaea, and eukaryotic organisms. Previous studies have suggested that HIV infection may be related to obvious changes in enteric bacterial populations (Dillon et al., 2014 2014 ; Dinh et al., 2015 2015 ; Monaco et al., 2016 2016 ). The bacterial microbiome includes Bifidobacterium , Lactobacillus , Escherichia coli , Enterococcus faecalis , and Enterococcus faecium . E. faecalis and E. faecium are commonly used in human intestinal colonization (Quiloan et al., 2012 2012 ). Lactobacillus and Bifidobacterium can prevent gastrointestinal infections and restore an effective intestinal barrier. They also have a positive effect on the immune function of HIV/AIDS patients (Irvine et al., 2010 2010 ). E . coli is the most common bacterium associated with diarrhea in HIV patients (Shah et al., 2016 2016 ). Moreover, bacterial microbiome alteration has been reported to be linked to inflammatory bowel disease (IBD) and inflammation in HIV-1 infection (Bäckhed et al., 2012 2012 ; Lyte, 2013 2013 ; Márquez et al., 2016 2016 ). However, a better understanding of the relationships established among inflammatory factors, CD4 + T lymphocyte counts, and the intestinal flora compartment in AIDS is urgently needed. In this study, we investigated the levels of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6), and the amounts of CD4 + T lymphocytes, E . coli , Lactobacillus , Bifidobacterium , E . faecalis , and E . faecium , as well as the correlations among them. Our results revealed that the intestinal microbiota of AIDS/HIV patients were disordered. The results also confirmed that there was a correlation between the amount of intestinal flora and the number of CD4 + T lymphocytes and levels of TNF-α and IL-6. The findings of our study may provide a new theoretical foundation for the clinical treatment of AIDS/HIV patients. Materials and methods 1 Patients and groups 2 Thirty AIDS/HIV patients (18 males and 12 females, aged 20–65 years) were included in the AIDS group. They were selected from the outpatient ( n =21) and inpatient ( n =9) departments of Qingdao Sixth People’s Hospital (Qingdao, China) from April 2016 to April 2018. The statistical characteristics of the patients are shown in Table 1 1 . Subjects who had used antacids within the previous two months were excluded. Patients with an active opportunistic infection or inflammation were also excluded from our cohort. Simultaneously, 30 healthy volunteers (15 males and 15 females, aged 23–61 years), were set as the control group. None of the volunteers had a history of gastrointestinal diseases or hepatobiliary diseases, and none had used antibiotics or microecological preparations within two months before the experiment. This study was approved by the Ethics Committee of Qingdao Sixth People’s Hospital and informed consent was signed by the patients and healthy volunteers. The values for HIV viral load are expressed as median (range) 2 Characteristics 2 Patients Number Percentage (%) Male 18 60.0 Female 12 40.0 Outpatient 21 70.0 Inpatient 9 30.0 Infection pathway  Drug abuse 10 33.3  Sexual transmission 16 53.4  Blood transmission 4 13.3 Antiretroviral therapy (ART)  Yes 10 33.3  No 20 66.7 Antibiotics  Yes 25 83.3  No 5 16.7 Acute illness  Yes 3 10.0  No 27 90.0 CD4 + cell count (cells/µL)  >500 5 16.7  200–500 15 50.0  <200 10 33.3 3 Median age (year) 2 39.5 Median CD4 + cell count (cells/µL) 2 304.5 HIV viral load * * (copies/mL plasma) 2  ART treatment 2 20 (0–50)  No treatment 2 95 672 (24 455–285 548) Detection of inflammatory factors by ELISA 2 Fasting venous blood samples (3–5 mL) were collected and stored at 4 °C, centrifuged at 2000 r/min for 10 min, and the plasma was dispensed into 2-mL Eppendorf (EP) tubes and stored at −80 °C. The levels of TNF-α and IL-6 were detected using an enzyme-linked immunosorbent assay (ELISA) kit (Cloud-Clone Corp., USA). The absorbance value was measured by an absorbance detector at 450 nm. Detection of CD4 + T lymphocytes by flow cytometry 2 The number of CD4 + T lymphocytes was assessed using a FACSCalibur type flow cytometer and a tricolor fluorescent antibody labeling kit (BD, USA), as described by Yao et al. ( 2017 2017 ) and Zhang SG et al. ( 2017 2017 ). According to the reagent specification, each sample was processed in a TruCONT tube dedicated to flow cytometry. A total of 20 µL of monoclonal antibody (mAb) was firstly added to the TruCONT tube, and then 50 μL of whole blood containing ethylenediaminetetraacetic acid (EDTA) was added. After 15 min in the dark, 450 μL of 10% (0.1 g/mL) fluorescence activated cell sorter (FACS) hemolysin was added and the tube was placed in the dark for 15 min. Finally, the number of CD4 + T lymphocytes was determined using MultiSET software. qRT-PCR 2 Fresh feces from the two groups were collected and placed on ice. A total of 220 mg of medium stool was weighed, and the fecal genomic DNA was extracted using a bacterial genomic DNA extraction kit (Tiangen Biochemical Technology Co., Ltd., Beijing, China). The DNA concentration of each sample was tested and adjusted to 20 µg/mL, and then the amounts of Bifidobacterium , Lactobacillus , E. coli , E. faecalis , and E. faecium in fecal samples were separately quantified by quantitative real-time polymerase chain reaction (qRT-PCR). Standards were set for simultaneous amplification in each reaction, and the DNA template was replaced with sterile ddH 2 O as a negative control. A total of 20 µL of reaction system was used for qRT-PCR, including 10 µL 2×SYBR mixture uracil- N -glycosylase (UNG; including reactive oxygen species (ROX)), 0.75 µL upstream and downstream primers, 2.0 µL DNA template, and 6.5 µL sterilized ddH 2 O. Then, the amplification was carried out according to the following procedures: UNG enzymes acted at 50 °C for 5 min, pre-denatured at 95 °C for 10 min followed by 35 cycles of 95 °C for 15 s, 60 °C for 15 s, and 72 °C for 30 s. The C T value and the standard curve were calculated as a quantitative result. The target gene sequence was searched from GenBank (https:// www www . ncbi.nlm.nih.gov), and primer design was carried out using Primer Premier 5.0 (Primer, Canada). Five primers were verified online by BLAST software (https://blast.ncbi.nlm.nih.gov/Blast.cgi) and synthesized by Shanghai Biotech Engineering Services Co., Ltd., Shanghai, China. The primer sequences are shown in Table 2 2 . F: forward; R: reverse Name Sequence (5'→3') 2 Bifidobacterium F: TCGCCTCCGGGTGAGAGTGG R: CGAAGCCATGGTGGGCCGTT 2 Lactobacillus F: TGGAAACAGGTGCTAATACCG R: GTCCATTGTGGAAGATTCCC 2 Escherichia coli F: CTCGCTGGCATTTGCGTAC R: ATCTTTTGCCGTCCGTTTTGG 2 Enterococcus faecalis F: TTGGCATTCCACAAGTACCA R: AATTGCTCGGGCATCATAAC 2 Enterococcus faecium F: TCGGACGACTTTGCCTGGCG R: TCGCACCGGCTCAATCCGC 2.5 Statistical analysis 2 The experimental measurements are expressed as mean±standard deviation (SD), and a sample t -test was performed using GraphPad Prism 5.0 software. The correlations between the amount of intestinal flora and the levels of TNF-α and IL-6 and the number of CD4 + T lymphocytes were analyzed by Spearman correlation. All experiments were carried out three times. If P < 0.05, statistical significance was accepted. Results 1 Study population characteristics 2 The median age of patients in the AIDS group was 39.5 years (range 20–65 years) and 60% were male. Drug abuse (33.3%), sexual transmission (53.4%), and blood transmission (13.3%) were the main routes of infection. Ten subjects (33.3%) in the AIDS group received ART treatment for six months, which consisted of tenofovir (20 mg/kg) and emtricitabine (30 mg/kg). In addition, 25 patients were treated with antibiotics consisting of vancomycin (15 mg/kg) and enrofloxacin (10 mg/kg) for one month. ART-treated participants had undetectable viral loads ( < 20 copies/mL plasma) and participants without ART treatment had high viral loads (95 672 copies/mL plasma). Three patients suffering acute illness were clinically diagnosed AIDS patients and the other 27 were HIV-positive patients, including patients not yet under treatment. Among the 30 patients, 10 (33.3%) had a CD4 + cell count of < 200 cells/µL, 15 (50.0%) had a CD4 + cell count of 200–500 cells/µL, and 5 (16.7%) had a CD4 + cell count of > 500 cells/µL. Three (10.0%) were suffering acute illness (Table 1 1 ). Higher levels of TNF-α and IL-6 in the peripheral blood of AIDS/HIV patients 2 The measured levels of inflammatory factors in the peripheral blood of the AIDS group and the control group are shown in Fig. 1 1 . TNF-α and IL-6 levels were markedly higher in subjects in the AIDS group than in the control group ( P < 0.05). The results illustrated that the expression of inflammatory factors in the peripheral blood of AIDS/HIV patients was abnormally high. (a) The expression level of IL-6; (b) The expression level of TNF-α. Data from experiments carried out three times are presented as mean±SD. * P < 0.05, vs. control Lower number of CD4 + T lymphocytes in AIDS/HIV patients 2 The numbers of CD4 + T lymphocytes in the AIDS and control groups are shown in Fig. 2 2 . The number of CD4 + T lymphocytes in the AIDS group was much lower than that in the control group ( P < 0.05), suggesting that the number of CD4 + T lymphocytes was abnormally low in AIDS/HIV patients. Data from experiments carried out three times are presented as mean±SD. * P < 0.05, vs. control Changes in the amounts of Bifidobacterium , Lactobacillus , E. coli , E. faecalis , and E. faecium 2 The relative amounts of Bifidobacterium and Lactobacillus in the AIDS group were markedly lower than those in the control group ( P < 0.05; Figs. 3a and 3b 3a and 3b ). However, the amounts of E. coli , E. faecalis , and E. faecium in the AIDS group were significantly higher than those in the control group ( P < 0.05; Figs. 3c–3e 3c–3e ). These findings indicated that the amounts of intestinal flora changed abnormally and the intestinal microbiota were destroyed. (a) Bifidobacterium ; (b) Lactobacillus ; (c) Escherichia coli ; (d) Enterococcus faecalis ; (e) Enterococcus faecium . Data from experiments carried out three times are presented as mean±SD. * P < 0.05, vs. control Correlations of the amount of intestinal flora with the levels of TNF-α and IL-6 in peripheral blood 2 Spearman correlation analysis showed that the amounts of Bifidobacterium and Lactobacillus in the AIDS group were negatively correlated with the level of TNF-α ( P < 0.05; Figs. 4a and 4b 4a and 4b ), while the amounts of E . coli , E . faecalis , and E . faecium were positively correlated with the level of TNF-α ( P < 0.05; Figs. 4c–4e 4c–4e ). Similarly, the amounts of Bifidobacterium and Lactobacillus in the AIDS group were negatively correlated with the level of IL-6 ( P < 0.05; Figs. 4f and 4g 4f and 4g ). In contrast, the amounts of E . coli , E . faecalis , and E . faecium were positively correlated with the level of IL-6 ( P < 0.05; Figs. 4h–4j 4h–4j ). Correlations between the content of Bifidobacterium and the level of TNF-α (a), Lactobacillus and the level of TNF-α (b), Escherichia coli and the level of TNF-α (c), Enterococcus faecalis and the level of TNF-α (d), Enterococcus faecium and the level of TNF-α (e), Bifidobacterium and the level of IL-6 (f), Lactobacillus and the level of IL-6 (g), E . coli and the level of IL-6 (h), E. faecalis and the level of IL-6 (i), E. faecium and the level of IL-6 (j) Correlations of the amount of intestinal flora with the number of CD4 + T lymphocytes in peripheral blood 2 The correlations between the intestinal flora and the number of CD4 + T lymphocytes were determined using Spearman correlation analysis. The results showed that the amounts of Bifidobacterium and Lactobacillus in the AIDS group were negatively correlated with the number of CD4 + T lymphocytes ( P < 0.05; Figs. 5a and 5b 5a and 5b ). In contrast, the amounts of E . coli , E . faecalis , and E . faecium in the AIDS group were positively correlated with the number of CD4 + T lymphocytes ( P < 0.05; Figs. 5c–5e 5c–5e ). Correlations between the number of CD4 + T lymphocytes and the content of Bifidobacterium (a), Lactobacillus (b), Escherichia coli (c), Enterococcus faecalis (d), Enterococcus faecium (e) Discussion 1 Intestinal parasitic infections and HIV/AIDS are major public health problems in developing countries, and are the main causes of high mortality rates (Gedle et al., 2017 2017 ). The progression of AIDS is a diverse process. Slow or rapid progression could present distinct behaviors of specific cell subpopulations and compartments, and components of the patient’s microbiota. HIV/AIDS is characterized by the targeting and destruction of CD4 + T lymphocytes in peripheral blood. Importantly, CD4 + T cells are the key to host defense and the primary driver of immune-mediated disease (O'Shea and Paul, 2010 2010 ; Zhang J et al., 2017 2017 ). In this study, the number of CD4 + T lymphocytes in peripheral blood was shown to be very low in AIDS/HIV patients. This was consistent with previous research which revealed that high levels of CD4 + T lymphocytes could improve the quality of life of AIDS patients (Taiwo et al., 2009 2009 ; Ren, 2018 2018 ). Immune activation has long been recognized as an important consequence of untreated HIV infection and a predictor of AIDS progression (Utay and Hunt, 2016 2016 ). In particular, IL-6, a pro-inflammatory cytokine, has a proinflammatory role in the regulation of immune responses (Hirano and Kishimoto, 1989 1989 ). Elevated levels of IL-6 can indicate a systemic inflammatory status, which is used as a marker of the HIV infection process (de Medeiros et al., 2016 2016 ). Sobti et al. ( 2010 2010 ) reported that suppressing IL-6 might decrease viral replication in the host after infection. TNF-α is an important mediator of inflammation and immune response (Fragoso et al., 2014 2014 ). The level of TNF-α is much higher in AIDS/HIV patients than in healthy people, and continuous changes of TNF-α levels might lead to tissue damage and contribute to the development of other diseases (de Pablo-Bernal et al., 2014 2014 ). In this study, levels of TNF-α and IL-6 were higher in the AIDS group, strongly suggesting that the progression of AIDS might be related to inflammatory response. Elevated IL-6 in HIV-infected patients was related to impeded recovery of low CD4 levels (Rosado-Sánchez et al., 2017 2017 ). CD4 is a T cell receptor for major histocompatibility complex class II antigens, a key regulator of immune response, and also a receptor for HIV (Wang et al., 1994 1994 ). Evidence suggests that poor CD4 + T lymphocyte recovery is associated with microbial translocation in HIV-infected patients (Ponte et al., 2016 2016 ). The enrichment of gut bacteria has been reported to be associated with poor CD4 + T cell reconstruction (Lu et al., 2018 2018 ). Previous studies have indicated that the composition of gut microbiota is related to cancer immunotherapy (Routy et al., 2018 2018 ) as well as HIV infection (Vujkovic-Cvijin et al., 2013 2013 ). The human gastrointestinal tract is a complex ecosystem inhabited by the microbiome, including bacteria, viruses, archaea, and eukaryotic organisms. Probiotics can improve intestinal barrier function and even enhance the immunity of HIV-infected individuals by reducing the duration of diarrhea (Monachese et al., 2011 2011 ). When the intestinal flora of AIDS patients is dysfunctional, the levels of Bifidobacterium and Lactobacillus are significantly lower, and the contents of E. coli , E. faecalis and E. faecium are higher (Lei et al., 2012 2012 ). Shah et al. ( 2016 2016 ) reported that E. coli is the most common bacterium associated with diarrhea in HIV patients. In addition, bacterial microbiome alteration is linked to IBD and inflammation in HIV-1 infection (Bäckhed et al., 2012 2012 ; Lyte, 2013 2013 ; Márquez et al., 2016 2016 ). In the current study, the amounts of Bifidobacterium and Lactobacillus were low and negatively correlated with TNF-α and IL-6, and the number of CD4 + T lymphocytes. The indications and correlations above in E. coli , E. faecalis , and E. faecium were exactly opposite to those of Bifidobacterium and Lactobacillus . Our results were consistent with those of previous studies. For example, He et al. ( 2014 2014 ) pointed out that the amount of Enterococcus in AIDS/HIV patients increased markedly, and CD4 + T lymphocyte counts were strongly and negatively correlated with Enterococcus counts. Li and Zhong ( 2017 2017 ) reported that the expression of inflammatory cytokines (IL-6 and TNF-α) in peripheral blood of patients with ulcerative colitis was higher than that of healthy people, and was negatively correlated with the contents of Bifidobacterium and Lactobacillus , but positively correlated with the contents of Enterobacter and Enterococcus . There were some limitations in our study. Firstly, our study was based on a small number of Chinese subjects and did not include people from other countries. Next, the effects of ART and antibiotic dosages and treatment regimens on the microbiome of AIDS/HIV patients were not investigated. These limitations will be addressed in our future research. 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