Molecular Vision 2014; 20:1137-1145 <>
Received 22 November 2013 | Accepted 01 August 2014 | Published 04 August 2014

Multiplex bead array assay of plasma cytokines in type 2 diabetes mellitus with diabetic retinopathy

Hui Hang, Songtao Yuan, Qin Yang, Dongqing Yuan, Qinghuai Liu

The first two authors contributed equally to this work.

Department of ophthalmology, The First Affiliated Hospital of Nanjing Medical University

Correspondence to: Qinghuai Liu, Department of ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China; Phone: 0086 025 83718836; FAX: 0086 025 83724440; email:


Purpose: The aim of this study was to assess the roles of plasma cytokines in diabetic retinopathy (DR) and their relationship with the severity of DR.

Methods: This study included 59 diabetic patients and 19 non-diabetic controls. The plasma concentrations of endothelial growth factor (EGF), eotaxin, fibroblast growth factor 2 (FGF-2), Flt-3 ligand (Flt-3L), fractalkine, granulocyte colony-stimulating factor (G-CSF), granulocyte–macrophage colony-stimulating factor (GM-CSF), growth-related oncogene (GRO), interferon (IFN)-α2, IFN-γ, interleukin (IL)-1α, IL-1β, IL-1Ra, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-12 (p40), IL-12 (p70), IL-13, IL-15, IL-17, IFN-inducible protein-10 (IP-10), monocyte chemoattractant protein (MCP)-1, MCP-3, macrophage-derived cytokine (MDC), macrophage inflammatory protein (MIP)-1α, MIP-1β, sCD40L, sIL-2Rα, transforming growth factor (TGF)-α, tumor necrosis factor (TNF)- α, TNF-β, and VEGF were measured with Luminex multiplex bead immunoassay. The levels of these cytokines were investigated according to the DR stage.

Results: The plasma level of ten cytokines—MCP-1, IL-6, IL-7, IL-9, IL-13, IL-15, IL-17, sCD40L, sIL-2Rα and TNF-β—increased significantly in the diabetic group compared to the controls. The Flt-3L, IL-1Ra, IL-3, IL-5, and IL-12 (p40) levels were lower in the diabetic group than in the control group. The TNF-α plasma level was significantly elevated in patients with proliferative diabetic retinopathy (PDR) compared with the levels in patients with non-proliferative diabetic retinopathy (NPDR) and patients with no apparent diabetic retinopathy (NDR).

Conclusions: TNF-α might be involved in the progression of DR, especially in the pathogenesis of PDR. TNF-α is a potential cytokine for the prognosis of DR and might act as a therapeutic target in DR.


Diabetic retinopathy (DR) is an important microvascular complication of diabetes mellitus (DM) and a common vision-threatening disease in the working-age population [1]. DR is characterized by retinal microvascular damage leading to vascular leakage and ischemia-induced retinal neovascularization through four classic pathways: the polyol pathway, increased advanced glycation end-product (AGE), protein kinase C (PKC) activation, and the superoxide pathway [2]. Activation of these pathways leads to upregulation of proangiogenic, immunologic, and inflammatory factors such as vascular endothelial growth factor (VEGF), tumor necrosis factor (TNF)-α, Flt-3 ligand (Flt-3L), interleukin (IL)-1β, IL-6, IL-8, sIL-2R, monocyte chemoattractant protein (MCP)-1, cyclooxygenase-2 (COX-2), IFN-inducible protein-10 (IP-10), and pigment epithelium-derived factor (PEDF) [1,3,4]. Researchers have conducted many studies on these factors, and VEGF has been studied extensively in the pathogenesis of DR. Although anti-VEGF therapy has been used in the clinical setting for many years [5], the etiology and pathogenesis of DR are complicated, and undoubtedly other potential components play important roles as well.

Inflammation is the potential component of DR investigated in the present study. Current discussions regarding inflammation include molecular changes and mechanisms. Many inflammatory cytokines have been found to be upregulated in the serum, vitreous humor, aqueous humor, and tear samples of patients with DR [6-10]. Studies aimed at understanding the mechanisms of inflammation have done by investigating cell signaling, animal models, and gene knockout. Results of these studies support the hypothesis that DR is a low-grade subclinical inflammatory disease.

Many cytokines play roles in DR and have multiple interactions that impact the pathogenesis of the disease. Therefore, studying only one cytokine is not enough. Multiplex bead array assay (MBAA) is a new technology that effectively allows multiple cytokines to be assayed from a single sample. Measurements using MBAA show excellent correlation with enzyme-linked immunosorbent assay (ELISA) data and reduce time, cost, sample volume, and sampling error [11]. This development is important, since other studies that have measured cytokines in the vitreous humor, aqueous humor, tears, and especially plasma of patients with DR have shown conflicting results [12]. To assess the roles of plasma cytokines in DR, we used MBAA to investigate the plasma levels of 39 cytokines in diabetic patients with DR compared with normal controls.


This study adhered to the ARVO statement on human subjects and was performed in compliance with the tenets of the Declaration of Helsinki and approved by the internal Ethics Committees of the First Affiliated Hospital of Nanjing Medical University. Written informed consent was obtained from every individual involved in this study.

Study population

This study recruited 59 patients with type 2 diabetes and 19 non-diabetic controls from the first affiliated hospital of Nanjing Medical University. The male to female ratio and mean±SD age in diabetic subjects was 23/36 and 61.8±5.3 years, and in the control group was 12/17 and 62.9±5.0 years. Dilated ophthalmic eye examinations, color fundus photography, and fluorescein fundus angiography were conducted on all subjects. According to the Diabetic Retinopathy Disease Severity Scale [13], the 59 diabetic patients were classified into three groups: 19 with no apparent retinopathy (NDR), 19 with non-proliferative diabetic retinopathy (NPDR), and 21 with proliferative diabetic retinopathy (PDR). The male to female ratio and mean±SD age was 9/10 and 64.1±4.0 in NDR, 6/13 and 60.6±5.7 in NPDR, and 8/13 and 60.8±5.5 in PDR.

At the time of recruitment, all the diabetic and control subjects were in well monitor and control of their state of health. Detailed demographic information was collected from every subject, such as family history, duration, current medication, height, weight, body mass index (BMI = weight/height2), blood pressure, and blood and urine samples. Fasting serum glucose, glycosylated hemoglobin (HbA1c), serum lipid, and serum creatinine levels were also recorded. Subjects with other systemic diseases apart from diabetes or with other ocular conditions, such as glaucoma, infection, uveitis, and previous ocular surgery history, were excluded.

Plasma collection

Blood samples (5 ml) were obtained from each subject by cubital venipuncture using anticoagulant tubes. After centrifugation at 1500 ×g for 15 min, the plasma samples were aliquoted and stored at −80 °C until further analysis.

Cytokine analysis

The plasma samples were analyzed using the MILLIPLEX Human Cytokine/Chemokine panel (catalog number MPXHCYTO60KPMX39 (premixed); Millipore Corporation, Billerica, MA). The kit can detect the following 39 cytokines simultaneously in a single sample: EGF, eotaxin, FGF-2, Flt-3L, fractalkine, G-CSF, GM-CSF, GRO, IFN- α2, IFN-γ, IL-1α,IL-1β, IL-1Ra, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-12 (p40), IL-12 (p70), IL-13, IL-15, IL-17, IP-10, MCP-1, MCP-3, MDC, MIP-1α, MIP-1β, sCD40L, sIL-2Rα, TGF-α, TNF-α, TNF-β, and VEGF.

The samples were brought to room temperature and added in duplicate to 96-well filter-bottom plates. Antibody-coated capture beads were added to the wells and incubated on a plate shaker at 4 °C overnight. After a washing step, the beads were further incubated with biotin-labeled secondary antibody for 1 h and then incubated with streptavidin–phycoerythrin for 30 min. Then 100 μl of sheath fluid were added to each well, and the samples were analyzed using Luminex laser-based fluorescent analytical test instrumentation (Luminex 200, Austin, TX). Cytokine concentrations were determined from standard curves prepared on each plate and expressed as picogram per milliliter (pg/ml).

Statistical analysis

The data were analyzed using the Statistical Package for Social Sciences (IBM SPSS Statistics 19.0, New York, NY). Differences between samples from two groups, such as diabetics and controls, were analyzed using the two-tailed Student t test or the two-tailed Mann–Whitney test, depending on normality assumptions and the homogeneity of variances. One-way ANOVA and the Kruskal–Wallis H test were used to evaluate differences among multiple groups, such as different degrees of DR severity. Spearman's rank order correlation was used to determine correlations between and to assess the association of clinical characteristics with cytokine levels. Univariate and multivariate logistic regression analysis was used to assess the risk factors for DR and PDR, which was estimated with odds ratios (ORs) with 95% confidence intervals (CIs). For all tests, p values less than 0.05 were considered significantly different.


Patients’ clinical characteristics

A total of 78 subjects with diabetes (cases, n = 59) and without diabetes (controls, n = 19) were included in the analysis. Clinical characteristics of the enrolled patients are shown in Table 1. The mean ± standard deviation (SD) age was 62.9±5.0 years in the controls, 64.1±4.0 years in the NDR group, 60.6±5.7 years in the NPDR group, and 60.8±5.5 years in the PDR group, with no significant difference among the groups (p = 0.093). The male to female ratio was 12:7 in the controls, 9:10 in the NDR group, 6:13 in the NPDR group, and 8:13 in the PDR group, with no significant difference (p = 0.232). The BMI was 21.9±1.6 in the controls, 23.0±2.5 in the NDR group, 23.2±2.8 in the NPDR group, and 24.0±2.4 in the PDR group, with no significant difference (p = 0.058). In the diabetic group, the mean±SD duration was 9.0±6.5 years in the NDR group, 11.3±6.5 years in the NPDR group, and 12.3±6.5 years in the PDR group (p = 0.266). The mean±SD HbA1c level was7.0±1.6% in the NDR group, 7.5±1.6% in the NPDR group, and 7.8±2.0% in the PDR group (p = 0.434; Table 1).

Expression of cytokines in plasma

The plasma levels of ten cytokines—MCP-1 (p = 0.020), IL-6 (p = 0.000), IL-7 (p = 0.000), IL-9 (p = 0.002), IL-13 (p = 0.000), IL-15 (p = 0.000), IL-17 (p = 0.004), sCD40L (p = 0.007), sIL-2Rα (p = 0.049), and TNF-β (p = 0.000)—were significantly higher in the diabetic group compared to the control group. Five factors—Flt-3L (p = 0.001), IL-1Ra (p = 0.000), IL-3 (p = 0.000), IL-5 (p = 0.000), and IL-12 (p40); (p = 0.000)—had lower levels in the diabetic group compared to the controls. When we subdivided the diabetic group into NDR, NPDR, and PDR groups, 13 of the 15 cytokines—all except MCP-1 (p = 0.061) and sIL-2Rα (p =0.123)—differed significantly among the control, NDR, NPDR, and PDR groups (p<0.05). TNF-α was also significantly different among the four groups (p = 0.005; Appendix 1). When multiple comparisons were examined, the TNF-α level was significantly higher in the PDR group compared to the NPDR and NDR groups (p = 0.009 and 0.001, respectively). There were no significant differences between any other two groups (PDR and control, p = 0.192; NDR and control, p = 0.055; NPDR and control, p = 0.245; NPDR and NDR, p = 0.401). The mean±SD TNF-α levels were 9.5±2.0 pg/ml in the control group, 7.1±1.8 pg/ml in the NDR group, 8.1±4.2 pg/ml in the NPDR group, and 11.1±4.5 pg/ml in the PDR group (Figure 1). There were no significant differences in the other 13 cytokines among the diabetic groups (NDR, NPDR, and PDR).

Logistic regression analysis

We subdivided the diabetic group into two groups: NDR (n = 19) and DR (NPDR and PDR groups, n = 40). A logistic regression analysis was used to assess the risk factors of DR, which included age, duration, HbA1c, and all the cytokines examined. A univariate analysis was used to screen out age, IL-2, IL-3, TNF-α, and TNF-β as related factors to DR; the ORs were 0.865 (p = 0.023), 0.451 (p = 0.038), 3.250 (p = 0.041), 1.301 (p = 0.039), and 0.078 (p = 0.016), respectively. A multivariate logistic forward regression analysis then excluded other factors except age (OR = 0.800, p = 0.023; Table 2). To evaluate the risk factors of PDR, we subdivided the diabetic group into two groups: no PDR (NDR and NPDR, n = 38) and PDR (n = 21). A univariate analysis was used to screen TNF-α, and IL-17 as related factors to PDR; the ORs were 1.31 (p = 0.013) and 0.45 (p = 0.038), respectively. A multivariate logistic forward regression analysis then excluded other factors except TNF-α (OR = 1.28, p = 0.025; Table 3).

Correlation analysis

The correlation between TNF-α and other cytokines was analyzed in the diabetic group and in the PDR group. TNF-α levels of the diabetic group correlated significantly with three cytokines: GRO (r = 0.419, p = 0.001), MIP-1β (r = 0.383, p = 0.004), and IL-8 (r = 0.377, p = 0.005; Figure 2). Furthermore in the PDR group, TNF-α levels correlated significantly only with GRO (r = 0.572, p = 0.008; Figure 3).


In our study, the plasma levels of ten cytokines—MCP-1, IL-6, IL-7, IL-9, IL-13, IL-15, IL-17, sCD40L, sIL-2Rα, and TNF-β—were higher in the diabetic group (n = 59) than in the control group (n = 19), while five cytokines—Flt-3L, IL-1Ra, IL-3, IL-5, and IL-12 (p40)—had lower levels in the diabetic group compared to the controls. Although 13 of the 15 cytokines were significantly different among the subdivided groups (control, NDR, NPDR, and PDR), there was no significant difference in these cytokines between any two diabetic groups (NDR, NPDR, and PDR) according to the multiple comparisons performed. When the diabetic groups were subdivided into NDR (n = 19) and DR (n = 40), there were no significant differences in any of the 15 cytokines between the groups. Thus, although these 15 cytokines play roles in DM, they do not contribute to DR.

TNF-α is the only cytokine assessed in this study that showed a relationship with DR. TNF-α was significantly higher in the PDR group compared with the NPDR and NDR groups. In addition, this was the first time the difference in TNF-α levels in PDR plasma was significant using the MBAA method. Lange [14] detected 42 cytokines (MBAA) in the plasma of PDR and control groups; the concentration of TNF-α was 4.94 (1.6–9.14) pg/ml in the PDR group and 6.45 (1.6–11.56) pg/ml in the controls, with no significant difference. Chen [15] (MBAA) also reported that TNF-α plasma levels were not significantly different between patients with DM and controls or within the different DR stages. However, studies support the results of the current study. Koleva-Georgieva [16] (using ELISA) reported that patients with PDR had significantly higher plasma TNF-α values compared with patients with NPDR. Evidence from other studies also supports our results. Kuo [17] reported that the sTNF-R1 and sTNF-R2 levels were highly correlated with the DR severity in patients with DM. Ben-Mahmud et al. [18] found that plasma or serum from diabetic patients with retinopathy increases the TNF-α-associated activity of cultured human myelocytic cells. In Paine et al.’s gene polymorphism analyses [19], the genetic variant TNF-α-238A was a potent risk factor for pathogenesis of PDR. Huang et al. [20], using the TNF-a knockout strain of mice, demonstrated that TNF-α has no effect on early breakdown of the blood–retinal barrier (BRB) in DR, but that it is essential for progressive BRB breakdown. All of these studies support the conclusion that TNF-α influences DR, especially in the progressive stages (PDR).

In this study, the average concentration of TNF-α in the control group was also at a relatively high level, higher than that in the NDR and NPDR groups, although without significant differences. We think that one reason for the variability of TNF-α expression in the control group is the sampling error, and another might be the effect of other undetected complications in the TNF-α level. The 19 non-diabetic controls were carefully screened to exclude any other systemic or eye disease; however, the screening did not completely eliminate the effect of some unknown status on the plasma level of TNF-α, since features of inflammation are displayed years before the onset of clinical manifestation. Enlarged sample size may reduce the impact of these potential elements and help us to get more credible results.

Many studies have investigated the mechanisms of action of TNF-α. TNF-α is the prototypical member of a family of cytokines that also include Fas ligand (FasL), CD40 ligand (CD40L), and TNF-related apoptosis-inducing ligand (TRAIL). It can induce apoptosis, differentiation, cell activation, and inflammation [21]. Aveleira [22] demonstrated that TNF-α increased the permeability of bovine retinal endothelial cells, decreased the protein and mRNA content of the tight junction proteins ZO-1 and claudin-5, and altered the cellular localization of these tight junction proteins. Preventing nuclear factor-kappa B (NF-ҡB) activation reduced TNF-α-stimulated permeability. Finally, inhibiting PKC reduced NF-ҡB activation and completely prevented alterations in the tight junction complex and cell permeability induced by TNF-α in cell culture and rat retinas. Joussen [21] found that the TNF-α inhibitor etanercept suppressed caspase activation, retinal cell injury, and apoptosis in short-term diabetic rats. Pericyte and endothelial cell loss was also reduced in long-term hypergalactosemic mice.

Univariate logistic regression analysis screened out age, TNF-β, and IL-2 as protective factors, while IL-3 and TNF-α were risk factors for DR. However, multivariate logistic forward regression analysis excluded the other factors, with the exception of age (OR = 0.800, p = 0.023), which is a protective factor in DR. The younger the patients with DM are, the more easily they may suffer DR. A clinic-based cross-sectional study in Singapore [23] also reported that younger age was a risk factor for vision-threatening retinopathy (multivariate OR = 0.97, p = 0.000). When considering the risk factors of PDR, a multivariate logistic forward regression analysis showed TNF-α (OR = 1.28, p = 0.025) as a risk factor in PDR. This result also supports our conclusion that TNF-α has a role in PDR. Because the pathogenesis of DR is complicated, a vast network of multiple factors affects DR [24]. Larger sample sizes would help better assess whether the cytokines studied are credible risk factors.

We are not aware of a previously reported association of TNF-α with GRO in the plasma of diabetes. GRO is a chemokine belonging to the CXC family, which recruits neutrophils and basophils and involves in the action of inflammation and angiogenesis [25]. Sajadi [26] found an elevated GRO level in the plasma of diabetic patients compared to the controls, and Lange [14] reported an increased expression of GRO in the vitreous of patients with PDR. From these reports and the result of our study, we assume that GRO may also be an influence factor in DR, especially in PDR, because it correlated with TNF-α, which was found to have a role in PDR, although the GRO itself in our study was not with significant difference among groups. There are evidence that the PKC and NF-ҡB pathways may be the common method for mediating the secretion or the mRNA expression of GRO and TNF-α [22,27]. A study in human vascular endothelial cells (ECs) revealed how TNF-α and GRO correlated; the study found that TNF-α stimulates GRO release from human ECs through c-Jun NH2-terminal kinase (JNK)-mediated GRO mRNA expression and p38 mitogen-activated protein kinase (MAPK)- and phosphatidylinositol 3-kinase (PI3K)-mediated GRO secretory processes [28]. Further investigation is needed to determine their relationship and to seek out the mechanisms in DR models.

VEGF has been extensively studied in the pathogenesis of DR. The concentration of VEGF in aqueous and vitreous humor in DR has been reported to be elevated in most studies, while there has been no consensus on the plasma level of VEGF [12]. Our results showed no significant differences among groups. In recent years, intravitreal injections of different types of anti-VEGF have been used in PDR and diabetic macular edema (DME). However, the effect of this treatment is not perfect, and response to the anti-VEGF treatments has been variable and transient. The regression rate of new vessels following anti-VEGF treatment has been shown to range from 62% to 87.5%; the average time before retinal neovascularization recurs has ranged from 2 weeks to 3 months [29,30]. This clinical observation indicates that many other factors in addition to VEGF might have roles in this process. Sfikakis et al. [31] conducted a double-blind, placebo-controlled, crossover, 32-week study in which patients with DME received the TNF-α inhibitor infliximab intravenously. The excess visual acuity in the infliximab-treated eyes was greater than that in the placebo-treated eyes, and the infliximab treatment was well tolerated. However, Pulido [32] and Wu [33] treated DME intravitreally with two TNF-α inhibitors, adalimumab and infliximab, and neither treatment appeared to benefit the affected eyes. TNF-α inhibitors might be useful therapeutic agents in treating DME in the future, either alone or in combination with the currently used anti-VEGF drugs. More well-designed trials are needed.

In conclusion, the increased plasma level of TNF-α in PDR indicates that TNF-α is involved in the pathogenesis of PDR. It is a potential cytokine as a therapeutic target of DR. Larger samples are needed to determine more related factors and their correlations with each other.

Appendix 1. Plasma concentration of 39 cytokines of each classification.


The study was supported by the National Natural Science Foundation of China (81070743 and 81001427) and a project funded by the priority academic program development of Jiangsu higher education institutions (JX10231801). The authors have no financial relationship with any organization and report no conflict of interest. This paper was presented at the Fifteenth National Conference on ocular fundus diseases (2013, Jinan, China), titled “Expression of 39 cytokines in DR patients.”


  1. Tang J, Kern TS. Inflammation in diabetic retinopathy. Prog Retin Eye Res. 2011; 30:343-58. [PMID: 21635964]
  2. Graves DT, Kayal RA. Diabetic complications and dysregulated innate immunity. Front Biosci. 2008; 13:1227-39. [PMID: 17981625]
  3. Doganay S, Evereklioglu C, Er H, Türköz Y, Sevinç A, Mehmet N, Savli H. Comparison of serum NO, TNF-alpha, IL-1beta, sIL-2R, IL-6 and IL-8 levels with grades of retinopathy in patients with diabetes mellitus. Eye (Lond). 2002; 16:163-70. [PMID: 11988817]
  4. Oh IK, Kim SW, Oh J, Lee TS, Huh K. Inflammatory and angiogenic factors in the aqueous humor and the relationship to diabetic retinopathy. Curr Eye Res. 2010; 35:1116-27. [PMID: 21121809]
  5. Rangasamy S, McGuire PG, Das A. Diabetic retinopathy and inflammation: novel therapeutic targets. Middle East Afr J Ophthalmol.. 2012; 19:52-9. [PMID: 22346115]
  6. Abu El-Asrar AM, Struyf S, Kangave D, Geboes K, Van Damme J. Chemokines in proliferative diabetic retinopathy and proliferative vitreoretinopathy. Eur Cytokine Netw. 2006; 17:155-65. [PMID: 17194635]
  7. Maier R, Weger M, Haller-Schober EM, El-Shabrawi Y, Wedrich A, Theisl A, Aigner R, Barth A, Haas A. Multiplex bead analysis of vitreous and serum concentrations of inflammatory and proangiogenic factors in diabetic patients. Mol Vis. 2008; 14:637-43. [PMID: 18385799]
  8. Liu J, Shi B, He S, Yao X, Willcox MD, Zhao Z. Changes to tear cytokines of type 2 diabetic patients with or without retinopathy. Mol Vis. 2010; 16:2931-8. [PMID: 21203348]
  9. Ozturk BT, Bozkurt B, Kerimoglu H, Okka M, Kamis U, Gunduz K. Effect of serum cytokines and VEGF levels on diabetic retinopathy and macular thickness. Mol Vis. 2009; 15:1906-14. [PMID: 19784389]
  10. Zhou J, Wang S, Xia X. Role of intravitreal inflammatory cytokines and angiogenic factors in proliferative diabetic retinopathy. Curr Eye Res. 2012; 37:416-20. [PMID: 22409294]
  11. Skogstrand K. Multiplex assays of inflammatory markers, a description of methods and discussion of precautions: Our experience through the last ten years. Methods. 2012; 56:204-12. [PMID: 22001645]
  12. Baharivand N, Zarghami N, Panahi F, Dokht Ghafari MY, Mahdavi Fard A, Mohajeri A. Relationship between vitreous and serum vascular endothelial growth factor levels, control of diabetes and microalbuminuria in proliferative diabetic retinopathy. Clin Ophthalmol.. 2012; 6:185-91. [PMID: 22331976]
  13. Wilkinson CP, Ferris FL, Klein RE, Lee PP, Agardh CD, Davis M, Dills D, Kampik A, Pararajasegaram R, Verdaguer JT, Global Diabetic Retinopathy Project Group. Proposed international clinical diabetic retinopathy and diabetic macular edema disease severity scales. Ophthalmology. 2003; 110:1677-82. [PMID: 13129861]
  14. Lange CA, Stavrakas P, Luhmann UF, de Silva DJ, Ali RR, Gregor ZJ, Bainbridge JW. Intraocular oxygen distribution in advanced proliferative diabetic retinopathy. Am J Ophthalmol. 2011; 152:406-12. [PMID: 21723532]
  15. Chen H, Wen F, Zhang X, Su SB. Expression of T-helper-associated cytokines in patients with type 2 diabetes mellitus with retinopathy. Mol Vis. 2012; 18:219-26. [PMID: 22312190]
  16. Koleva-Georgieva DN, Sivkova NP, Terzieva D. Serum inflammatory cytokines IL-1beta, IL-6, TNF-alpha and VEGF have influence on the development of diabetic retinopathy. Folia Med (Plovdiv). 2011; 53:44-50. [PMID: 21797106]
  17. Kuo JZ, Guo X, Klein R, Klein BE, Cui J, Rotter JI, Ipp E, Chen YD. Systemic soluble tumor necrosis factor receptors 1 and 2 are associated with severity of diabetic retinopathy in Hispanics. Ophthalmology. 2012; 119:1041-6. [PMID: 22330960]
  18. Ben-Mahmud BM, Mann GE, Datti A, Orlacchio A, Kohner EM, Chibber R. Tumor necrosis factor-alpha in diabetic plasma increases the activity of core 2 GlcNAc-T and adherence of human leukocytes to retinal endothelial cells: significance of core 2 GlcNAc-T in diabetic retinopathy. Diabetes. 2004; 53:2968-76. [PMID: 15504978]
  19. Paine SK, Sen A, Choudhuri S, Mondal LK, Chowdhury IH, Basu A, Mukherjee A, Bhattacharya B. Association of tumor necrosis factor α, interleukin 6, and interleukin 10 promoter polymorphism with proliferative diabetic retinopathy in type 2 diabetic subjects. Retina. 2012; 32:1197-203. [PMID: 22105495]
  20. Huang H, Gandhi JK, Zhong X, Wei Y, Gong J, Duh EJ, Vinores SA. TNFα is required for late BRB breakdown in diabetic retinopathy, and its inhibition prevents leukostasis and protects vessels and neurons from apoptosis. Invest Ophthalmol Vis Sci. 2011; 52:1336-44. [PMID: 21212173]
  21. Joussen AM, Doehmen S, Le ML, Koizumi K, Radetzky S, Krohne TU, Poulaki V, Semkova I, Kociok N. TNF-α mediated apoptosis plays an important role in the development of early diabetic retinopathy and long-term histopathological alterations. Mol Vis. 2009; 15:1418-28. [PMID: 19641635]
  22. Aveleira CA, Lin CM, Abcouwer SF, Ambrosio AF, Antonetti DA. TNF-α Signals Through PKCζ/NF-ҡB to Alter the Tight Junction Complex and Increase Retinal Endothelial Cell Permeability. Diabetes. 2010; 59:2872-82. [PMID: 20693346]
  23. Lim MC, Lee SY, Cheng BC, Wong DW, Ong SG, Ang CL, Yeo IY. Diabetic retinopathy in diabetics referred to a tertiary centre from a nationwide screening programme. Ann Acad Med Singapore. 2008; 37:753-9. [PMID: 18989491]
  24. Shen X, Zhang Q. Network of multiple factors and cascades: hotspots of mechanism studies for diabetic retinopathy. Chin J Ocul Fundus Dis.. 2013; 29:5-8.
  25. Schoenberger SD, Kim SJ, Sheng J, Rezaei KA, Lalezary M, Cherney E. Increased prostaglandin E2 (PGE2) levels in proliferative diabetic retinopathy, and correlation with VEGF and inflammatory cytokines. Invest Ophthalmol Vis Sci. 2012; 53:5906-11. [PMID: 22871833]
  26. Sajadi SM, Khoramdelazad H, Hassanshahi G, Rafatpanah H, Hosseini J, Mahmoodi M, Arababadi MK, Derakhshan R, Hasheminasabzavareh R, Hosseini-Zijoud SM, Ahmadi Z. Plasma levels of CXCL1 (GRO-alpha) and CXCL10 (IP-10) are elevated in type 2 diabetic patients: evidence for the involvement of inflammation and angiogenesis/angiostasis in this disease state. Clin Lab. 2013; 59:133-7. [PMID: 23505918]
  27. Quan Y, Du J, Wang X. High glucose stimulates GRO secretion from rat microglia via ROS, PKC, and NF-kappaB pathways. J Neurosci Res. 2007; 85:3150-9. [PMID: 17639599]
  28. Lo HM, Lai TH, Li CH, Wu WB. TNF-α induces CXCL1 chemokine expression and release in human vascular endothelial cells in vitro via two distinct signaling pathways. Acta Pharmacol Sin. 2014; 35:339-50. [PMID: 24487964]
  29. Avery RL. Regression of retinal and iris neovascularization after intravitreal bevacizumab (Avastin) treatment. Retina. 2006; 26:352-4. [PMID: 16508438]
  30. Spaide RF, Fisher YL. Intravitreal bevacizumab (Avastin) treatment of proliferative diabetic retinopathy complicated by vitreous hemorrhage. Retina. 2006; 26:275-8. [PMID: 16508426]
  31. Sfikakis PP, Grigoropoulos V, Emfietzoglou I, Theodossiadis G, Tentolouris N, Delicha E, Katsiari C, Alexiadou K, Hatziagelaki E, Theodossiadis PG. Infliximab for diabetic macular edema refractory to laser photocoagulation: a randomized, double-blind, placebo-controlled, crossover, 32-week study. Diabetes Care. 2010; 33:1523-8. [PMID: 20413522]
  32. Pulido JS, Pulido JE, Michet CJ, Vile RG. More questions than answers: a call for a moratorium on the use of intravitreal infliximab outside of a well-designed trial. Retina. 2010; 30:1-5. [PMID: 20061905]
  33. Wu L, Hernandez-Bogantes E, Roca JA, Arevalo JF, Barraza K, Lasave AF. Intravitreal tumor necrosis factor inhibitors in the treatment of refractory diabetic macular edema: a pilot study from the Pan-American Collaborative Retina Study Group. Retina. 2011; 31:298-303. [PMID: 21099452]