- Research article
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Serological cytokine profiles of cardiac rejection and lung infection after heart transplantation in rats
Journal of Cardiothoracic Surgeryvolume 14, Article number: 26 (2019)
Allograft rejection and infection are the major sources of morbidity and mortality after heart transplant. Early differential diagnosis is clinically crucial but difficult. The aim of the study was to examine serum cytokine profiles associated with each entity and whether such profiles could help to differentiate between them.
Heart allografts from Wistar rats were transplanted to Lewis rats as described by Yokoyama. Cardiac rejection and pulmonary bacterial infection were induced by Cyclosporine cessation and bacteria bronchus injection, and pathologically confirmed. Ninety serological cytokines profiles of the study objects were then simultaneously measured using a biotin label-based cytokine array. The fold change (FC) was used for relative cytokine concentration comparison analysis.
Four cytokines in cardiac rejection group were significantly dysregulated as compared to health controls (β -Catenin, 0.51 FC; E-Selectin, 0.62 FC; IFN-gamma, 1.87 FC; and IL-13, 0.60 FC, respectively). In pulmonary infection animals, 11 cytokines were remarkably dysregulated in comparison with the control group (CINC-3, 0.57 FC; CNTF R alpha, 0.59 FC; E-Selectin, 0.58 FC; FSL1,0.62 FC; Hepassocin, 0.64 FC; IL-2, 0.26 FC; IL-13, 0.49 FC; NGFR, 0.57 FC; RAGE, 0.50 FC; TIMP-1, 0.49 FC; and IFN-gamma, 1.77 FC, respectively). Eleven cytokines were significantly up-regulated in cardiac rejection group comparing to the pulmonary infection animals (FSL1, 2.32FC; Fractalkine, 1.65FC; GFR alpha-1, 1.64FC; IL-2, 2.72FC; IL-5, 1.60FC; MMP-2, 1.71FC; NGFR, 2.25FC; TGF-beta1, 1.58FC; TGF-beta3, 1.58FC; Thrombospondin, 1.64FC, and TIMP-1, 1.52FC, respectively).
The current study illustrated the disease-specific serological cytokine profiles of allograft rejection and pulmonary bacterial infection after cardiac transplant. Such disease associated cytokine portraits might have the potential for early discrimination diagnosis.
Heart transplantation remains the only established cure for patients suffer from end-stage cardiac diseases. Acute cardiac allograft rejection and infection are the major causes of death for cardiac transplanted patients, accounting for almost 40% reported deaths within the first year after the surgery . The clinical therapy of rejection and infection is closely intertwined, immunosuppression to prevent or treat rejection can increase the risk of infection; tapering off immunosuppressant to treat infection can exacerbate rejection. As both entities present with similar, non-specific symptoms such as dysponea, fatigue, and low-grade fever at disease onset, their early discrimination is critical yet challenging.
Expression profiling has the potential not only to identify disease biomarkers, but also may provide mechanism insights. Studies have utilized either genomics or proteomics to examine heart rejection [2, 3]. However little has been done to investigate the complex pathophysiology and underlying mechanisms of cardiac rejection and infection that complicating heart transplant. Using an animal model of lung bacterial infection after heterotopic cardiac transplantation we have recently developed , the current study simultaneously examined ninety serological cytokines profiles in the course of acute cardiac rejection and pulmonary infection with a biotin-labeled-based cytokine protein array system. Our hypotheses are 1) disease-specific cytokine pattern exists in each entity, and 2) such cytokine patterns might have the potential to aid differential diagnosis.
Inbred Wistar (donor) and Lewis (recipient) rats, male, weighing 200–250 g, were purchased from Slac Laboratory (Shanghai, China), maintained in the animal facility of Zhongshan hospital, Fudan University under standard conditions, and allowed to drink water and eat rodent chow ad libitum. The current study was approved by the Animal Care and Use Committee (ACUC) of Zhongshan hospital, Fudan University. Animal care followed the criteria of the ACUC of the NIH. Throughout the study, every effort was taken to minimize any suffering of the animals.
Heterotopic cardiac transplantation
Cardiac allograft rejection and pulmonary bacterial infection were induced as the following . Cardiac transplantations were performed using a modified version of the heterotopic cardiac transplantation model reported by Yokoyama et al . In brief, animals were anesthetized with 40 mg/kg of intraperitoneal injection of pentobarbital. After heparinization, donor heart was procured in the conventional fashion. After flushing the coronary circulation with 10 ml of cold lactated Ringers solution, donor heart was placed in iced lactated Ringers solution where the donor heart was tailored by the ligation of main pulmonary artery, superior vena and inferior vena cave (IVC), and the removal of tricuspid valve and interatrial septum. After such preparations, donor hearts were replaced in iced lactated Ringers solution while the recipient animals were prepared. The IVC and abdominal aorta of the recipient animals are exposed through a longitudinal laparotomy with a left subcostal take-off. The donor ascending aorta was then anastamosed to the recipient abdominal aorta with a running 8–0 prolene. Similarly, the donor right atrium was anastamosed to the recipient IVC. Consequently, the left atrium and ventricle of graft were loaded with the blood from the right atrium through the interatrial communication. Upon re-establishment of blood flow, transplanted heart resumed spontaneous contractions in sinus rhythm, and was free of gross surgical injury at the time of closure.
Induction of pulmonary infection
Via a tracheostomy, 0.2 ml of Pseudomonas aeruginosa ATCC 27853 (1 × 109 CFUs/ml, American Type Culture Collection, Manassas, VA) was injected into the stem bronchus of recipient animals assigned to the infection group under direct vision to induce bacterial pneumonia. For non-infection animals, 0.2 ml of normal saline was injected into the stem bronchus of recipient rats under direct vision.
Animal grouping and sample procurement
All recipient animals were begun on daily cyclosporine A (CSA) subcutaneous injection (10 mg/kg/day) to suppress rejection. On post-operative day (POD) 6, recipient animals were randomized to either have their CSA continued, or have their CSA discontinued and began on a normal saline placebo injection (10 mg/kg/day subcutaneously, rejection group, n = 7). On POD 13, non-rejection animals were further randomized to either receiving intratracheal inoculation of Pseudomonas aeruginosa (infection group, n = 7), or receiving intratracheal inoculation of normal saline (control group, n = 7). Animals of the rejection group also received intratracheal inoculation of normal saline on POD 13 (Fig. 1).
Graft viability was assessed daily by palpation of the donor heart. Rejection was defined as cessation of a palpable heartbeat and was confirmed by direct inspection at laparotomy upon organ harvest. Animals were sacrificed on POD 14, lungs and transplanted hearts were procured after blood withdrawals. Cross-sections of heart and lung were processed for histopathology using hematoxylin and eosin staining. Histological changes were blindly assessed by a pathologist, allograft rejections were evaluated using the International Society of Heart and Lung Transplantation (ISHLT) system for rejection .
Measurement of cytokines
Upon harvest on POD 14, peripheral blood samples were withdrawal from all recipient animals. After being allowed to clot at room temperature for 1 h, blood samples were centrifuged at 1500×g for 10 min, sera were then collected and stored at − 80 °C until use.
Serum levels of 90 cytokines were measured by RayBio Biotin Label-based Rat Antibody Array 1 (RayBiotech, Norcross, GA, USA) follow the recommended protocol from manufacture. In brief, sample mixtures consist of serum aliquots from the same study groups were biotinylated and dialyzed for incubation with the array. These samples were then added to the array membrane and incubated at room temperature. After incubation with HRP-stretavidin, the signals were visualized by exposure to x-ray film with subsequent development. Cytokines of interest were quantified by densitometry using ImageJ software (http://imagej.net). By subtracting the background staining immediately surrounding each sample and normalizing to the positive controls on the same membrane, the relative protein concentrations were obtained. In precaution of inter-assay variations, cytokines levels were measured using cytokine array kit from the same shipment, and performed under the same laboratory conditions.
Samples with cytokine levels below the detection limits were arbitrarily assigned the values corresponding to the minimum limits. Per manufacture’s instruction (https://www.raybiotech.com/files/manual/Antibody-Array/AAR-BLG-1.pdf), the relative protein concentration of cytokine was used for comparison analysis. Each cytokine was compared between groups in fold change (FC). A FC of 1.50 or greater represents significant up-regulation, and FC of 0.65 or less represents significant down-regulation.
Induction of allograft rejection and pulmonary infection
The mean total transplant operation time was 55 min (range, 48–65 min). The mean ischemic time of donor hearts was 35 min (range, 31–47 min). The allograft heartbeat of the non-rejection animals remained energetic throughout the study period, while the transplanted heart gradually lost its contractions over time after CSA cessation in the rejection group. Major morbidities of myocardial infarction (n = 1, rejection group; n = 2, control group, respectively) and thrombosis (n = 1, rejection group) were detected by direct observation and histopathology, and these 4 animals were excluded from the study. The remaining 17 animals (n = 5, rejection group; n = 7, infection group; and n = 5, control group, respectively) were processed for further analysis.
Histological evaluation of cardiac allografts of the non-rejection group revealed minimal histologic changes with no evidence of interstitial edema or inflammation (ISHLT grade 0 R). In rejection group, however, severe rejection (ISHLT grade 3 R) were confirmed with diffuse inflammatory process and necrosis normal staining patterns observed on the tissue sections.
Similarly, minimal histological changes were found in the non-infection animal lung sections, while animals of the infection group had severe pneumonia with typical changes such as alveolar septal congestion, edema, focal alveolar hemorrhage, and infiltration of neutrophils and macrophages.
Cytokine portraits in cardiac rejection animals
Serum levels of 90 cytokines were analyzed simultaneously. The statistic significant differences were reached in 4 cytokines in rejection group as compared to the control group (beta-Catenin, 0.51 FC; E-Selectin, 0.62 FC; IFN-gamma, 1.87 FC; and IL-13, 0.60 FC, respectively) (Fig. 2). Of them, beta-Catenin, E-Selectin, and IL-13 were significantly down-regulated in the rejection group whereas serum level of IFN-gamma was remarkably up-regulated in the rejection group.
Cytokine portraits in pulmonary infection animals
The statistic significant differences were reached in 11 cytokines when infection animals comparing to the health controls. Of them, 10 cytokines (CINC-3, CNTF R alpha, E-Selectin, FSL1, Hepassocin, IL-2, IL-13, NGFR, RAGE, and TIMP-1) were significantly down-regulated (CINC-3, 0.57 FC; CNTF R alpha, 0.59 FC; E-Selectin, 0.58 FC; FSL1,0.62 FC; Hepassocin, 0.64 FC; IL-2, 0.26 FC; IL-13, 0.49 FC; NGFR, 0.57 FC; RAGE, 0.50 FC; and TIMP-1, 0.49 FC, respectively), while IFN-gamma were up-regulated in the rejection group (1.77 FC) (Fig. 2).
Differential cytokine patterns between cardiac rejection animals and pulmonary infection animals
Eleven cytokines (FSL1, Fractalkine, GFR alpha-1, IL-2, IL-5, MMP-2, NGFR, TGF-beta1, TGF-beta3, Thrombospondin, and TIMP-1) were found significantly up-regulated in cardiac rejection animals comparing to the pulmonary infection ones (Fig. 3). Of them, IL-2 exhibited the highest up-regulation with a fold increase of 2.72, followed by FSL1 (2.32 FC), and NGFR (2.25 FC). While the levels of IFN-gamma, IL-13 and E-Selectin were statistically dysregulated in both groups of rejection (1.87 FC, 0.60FC, and 0.62 respectively) and infection (1.77FC, 0.49FC, and 0.58, respectively) when compared to the health controls, no difference was found between the groups of rejection and infection, although numerically higher in the rejection group (1.06 FC, 1.24FC, and 1.08FC, respectively, in comparison with infection group) (Fig. 2).
Allograft rejection and infection are the leading causes of death after heart transplantation, ranks 4th and 1st respectively during the first year after the surgery, according to the latest ISHLT adult heart transplantation annual report . Although treatment targeting rejection and infection have being continuously explored, the clinical outcomes remain unsatisfying. As both entities present with similar, nonspecific symptoms at early stage, it is difficult for timely discrimination, which lead to misdiagnosis and therapy delay. Endomyocardial biopsy as the gold standard for cardiac rejection, is invasive and biased. Although transcript expression profiling of peripheral blood has been reported for cardiac rejection surveillance, however little has been done to explore the potential role of serologic cytokine profiling to discriminate between infection and allograft rejection.
The assessment of 90 cytokines revealed 4 proteins (beta-Catenin, E-Selectin, IFN-gamma, and IL-13) in the serum of cardiac allograft rejection animals, and 11 proteins (CINC-3, CNTF R alpha, E-Selectin, FSL1, Hepassocin, IL-2, IL-13, NGFR, RAGE, IFN-gamma, and TIMP-1) in the serum of bacterial pulmonary infection animals that were remarkably dysregulated in comparison with the health controls. These results suggest that distinctive serum protein portraits do exist in allograft rejection and infection in the context of cardiac transplantation. Furthermore, levels of FSL1, Fractalkine, GFR alpha-1, IL-2, IL-5, MMP-2, NGFR, TGF-beta1 and -beta3, Thrombospondin, and TIMP-1 were significantly up-regulated in cardiac rejection animals in comparison with the pulmonary infection animals. However, none of them could differentiate rejection animals from health controls. These findings support our hypothesis that serological cytokine profiling might have the potential to differentiate between infection and rejection.
In the panel of cytokines that differentiates between infection and rejection, IL-2 exhibited the highest fold increase. Originally identified as a T cell growth factor, IL-2 is known to play a dual role in induction or suppression of immune responses via activation of conventional and regulatory T cells . Researchers have found that IL-2 is increased in heart transplant patients and is specifically involved in cardiac rejection [8, 9]. During cardiac rejection, IL-2 mRNA and protein are predominantly produced by graft-infiltrating lymphocytes . Its intracellular expression and soluble production has the potential to be served as a predictive biomarker for acute rejection and personal drug response .
FSL1 and NGFR succeed IL-2 as the top 3 remarkably increased cytokines rejection vs infection. FSL1 is a secreted glycoprotein produced expressed in various tissues. The essential biological function of FSL1 is binding and neutralizing transforming growth factor beta (TGF-beta) superfamily, enhancing synthesis of proinflammatory cytokines and chemokines by immune cells. FSL1 is elevated in various inflammatory conditions and decreased during the course of treatment, it may therefore be a valuable biomarker for such diseases [12, 13]. Its dysregulated expression postulate its potential role in contributing to allograft dysfunction following lung transplantation [14, 15]. The activity of the heart is widely regulated by its autonomous nervous system, however this important mechanism of control is lost in the transplanted heart. NGFR is reported to play key role in restoring innervation of the cardiac allograft, as such its upregulation might be a response to the impairment of the allograft nervous system caused by immune-rejection .
Serum levels of Fractalkine, GFR alpha-1, IL-5, MMP-2, TGF-beta1, TGF-beta3, Thrombospondin, and TIMP-1 were also up-regulated in rejection animals than those in infection animals. Among them, Fractalkine belongs to the chemokine family whose expression was found negligible in nonrejecting cardiac isografts but was significantly enhanced in rejecting allografts, its blockage significantly prolonged allograft survival, suggesting a critical role for Fractalkine in in the pathogenesis of acute rejection [17,18,19]. GFR alpha-1 is a coreceptor that recognizes the GDNF family of ligands and has been implicated in the regulation of neuronal cell survival and differentiation. It has a role in the progression and metastasis of human cancers in that it promotes migration and invasion [20, 21], however its role in cardiac rejection remains unclear. IL-5 plays an essential role in inflammation and the allergic response, favoring the production, maturation, proliferation, recruitment, differentiation, and survival of eosinophils. Over-expression of IL-5 significantly increases eosinophil numbers and antibody levels, its critical role has long been recognized in allograft rejection [22, 23]. IL-5 blockade with anti-IL-5 antibody could prevent chronic rejection of cardiac grafts . MMP-2, a type IV collagenase, which facilitates tissue invasion of leukocytes and exerts a direct pro-inflammatory effect upon glomerular meningeal cells, has been implicated in allograft rejection [25,26,27]. TGF beta is a key cytokine important in acute inflammation, it plays a central role in both the initiation and propagation of acute and chronic rejection in the acute rejection episodes of solid organ transplant recipients, TGF-β antibody has been reported to be capable in preventing allografts rejection [28,29,30]. Known to play an important role in activating TGF-β, Thrombospondin has long been considered a potent modulator of allografts rejection [31,32,33]. TIMP-1, a natural inhibitor of the MMPs, is also a key modulator in immune-rejection .
This study has several acknowledged limitations. As this is an observation study, future functional experiments are needed to investigate the underlying mechanism of specific cytokine related to the diseases. In addition, as this is an exploratory study, multiple testing in precaution of type I error should be performed in future study to validate the results. Furthermore, only a small fraction of cytokines was tested in this study, while it is known that there are hundreds or thousands molecules involved in the immunological responses of rejection and infection. Lastly, the current study evaluated the cytokine profiles statically for only one time-point, as the immunological responses of rejection and infection are complex and dynamically, the current findings should be further monitored and evaluated at different stages and time-points during development of diseases.
This preliminary study demonstrated the disease-specific serological cytokine portraits in cardiac allograft rejection and pulmonary bacterial infection after heart transplant. A panel of serum cytokines that might have the potential to discriminate between cardiac rejection and lung infection was also identified. However the specific cytokine pathways and underlying mechanisms need further investigation.
Animal Care and Use Committee
Cytokine-induced neutrophil chemoattractant 3
- CNTF R Alpha:
ciliary neurotrophic factor receptor alpha
- GFR alpha-1:
glial cell line derived neurotrophic factor family receptor alpha 1
International Society of Heart and Lung Transplantation
inferior vena cava
Matrix metallopeptidase 2
Nerve growth factor receptor
Advanced glycosylation end-product specific receptor
Transforming growth factor beta 1
Transforming growth factor beta 3
TIMP metallopeptidase inhibitor 1
Lund LH, Khush KK, Cherikh WS, Goldfarb S, Kucheryavaya AY, Levvey BJ, et al. The registry of the International Society for Heart and Lung Transplantation: thirty-fourth adult heart transplantation Report-2017; focus theme: allograft ischemic time. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 2017;36(10):1037–46.
Bao Y, Xiu DR, Zhang L. Proteomic profiling of heterotopic heart-transplanted rats using surface-enhanced laser desorption/ionization time-of-flight mass spectrometry: potential biomarkers and drug targets. The Journal of international medical research. 2013;41(3):628–35.
Crespo-Leiro MG, Stypmann J, Schulz U, Zuckermann A, Mohacsi P, Bara C, et al. Clinical usefulness of gene-expression profile to rule out acute rejection after heart transplantation: CARGO II. Eur Heart J. 2016;37(33):2591–601.
Chen H, Yu W, Lu C, Zhan Y, Cheng Y. Mei Y. A rat model of pulmonary infection after cardiac transplant. Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation. 2015;13(2):167–72.
Yokoyama H, Ohmi M, Murata S, Nakame T, Tabayashi K, Mohri H. Proposal of a working left heart model with a heterotopic transplantation technique in rats. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 1995;14(4):706–12.
Stewart S, Winters GL, Fishbein MC, Tazelaar HD, Kobashigawa J, Abrams J, et al. Revision of the 1990 working formulation for the standardization of nomenclature in the diagnosis of heart rejection. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 2005;24(11):1710–20.
Mitra S, Leonard WJ. Biology of IL-2 and its therapeutic modulation: mechanisms and strategies. J Leukoc Biol. 2018.
van Emmerik N, Baan C, Vaessen L, Jutte N, Quint W, Balk A, et al. Cytokine gene expression profiles in human endomyocardial biopsy (EMB) derived lymphocyte cultures and in EMB tissue. Transplant international : official journal of the European Society for Organ Transplantation. 1994;7(Suppl 1):S623–6.
Wu CJ, Kurbegov D, Lattin B, Burchard E, Finkle C, Valantine H, et al. Cytokine gene expression in human cardiac allograft recipients. Transpl Immunol. 1994;2(3):199–207.
Baan CC, van Besouw NM, Daane CR, Balk AH, Mochtar B, Niesters HG, et al. Kinetics of IL-2 and IL-4 mRNA and protein production by graft-infiltrating lymphocytes responsible for rejection after clinical heart transplantation. Transpl Immunol. 1997;5(2):97–103.
Millan O, Rafael-Valdivia L, Torrademe E, Lopez A, Fortuna V, Sanchez-Cabus S, et al. Intracellular IFN-gamma and IL-2 expression monitoring as surrogate markers of the risk of acute rejection and personal drug response in de novo liver transplant recipients. Cytokine. 2013;61(2):556–64.
Chaly Y, Hostager B, Smith S, Hirsch R. Follistatin-like protein 1 and its role in inflammation and inflammatory diseases. Immunol Res. 2014;59(1–3):266–72.
Zhang L, Liu K, Han B, Xu Z, Gao X. The emerging role of follistatin under stresses and its implications in diseases. Gene. 2018;639:111–6.
Westall GP, Snell GI, Loskot M, Levvey B, O'Hehir R, Hedger MP, et al. Activin biology after lung transplantation. Transplantation direct. 2017;3(6):e159.
Snell JN, Westall GP, Snell GI. The potential role of activin and follistatin in lung transplant dysfunction. Expert review of respiratory medicine. 2015;9(6):697–701.
Galli A. Can the nerve growth factor promote the reinnervation of the transplanted heart? Med Hypotheses. 2014;82(2):229–30.
Robinson LA, Nataraj C, Thomas DW, Howell DN, Griffiths R, Bautch V, et al. A role for fractalkine and its receptor (CX3CR1) in cardiac allograft rejection. Journal of immunology (Baltimore, Md : 1950). 2000;165(11):6067–72.
Haskell CA, Hancock WW, Salant DJ, Gao W, Csizmadia V, Peters W, et al. Targeted deletion of CX(3)CR1 reveals a role for fractalkine in cardiac allograft rejection. J Clin Invest. 2001;108(5):679–88.
Imai T, Yasuda N. Therapeutic intervention of inflammatory/immune diseases by inhibition of the fractalkine (CX3CL1)-CX3CR1 pathway. Inflammation and regeneration. 2016;36:9.
Bhakta S, Crocker LM, Chen Y, Hazen M, Schutten MM, Li D, et al. An anti-GDNF family receptor alpha 1 (GFRA1) antibody-drug conjugate for the treatment of hormone receptor-positive breast Cancer. Mol Cancer Ther. 2017.
Kim M, Jung JY, Choi S, Lee H, Morales LD, Koh JT, et al. GFRA1 promotes cisplatin-induced chemoresistance in osteosarcoma by inducing autophagy. Autophagy. 2017;13(1):149–68.
Le Moine A, Flamand V, Demoor FX, Noel JC, Surquin M, Kiss R, et al. Critical roles for IL-4, IL-5, and eosinophils in chronic skin allograft rejection. J Clin Invest. 1999;103(12):1659–67.
Braun MY, Desalle F, Le Moine A, Pretolani M, Matthys P, Kiss R, et al. IL-5 and eosinophils mediate the rejection of fully histoincompatible vascularized cardiac allografts: regulatory role of alloreactive CD8(+) T lymphocytes and IFN-gamma. Eur J Immunol. 2000;30(5):1290–6.
Chen Y, Li D, Tsang JY, Niu N, Peng J, Zhu J, et al. PPAR-gamma signaling and IL-5 inhibition together prevent chronic rejection of MHC class II-mismatched cardiac grafts. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 2011;30(6):698–706.
Ermolli M, Schumacher M, Lods N, Hammoud M, Marti HP. Differential expression of MMP-2/MMP-9 and potential benefit of an MMP inhibitor in experimental acute kidney allograft rejection. Transpl Immunol. 2003;11(2):137–45.
Kuyvenhoven JP, Verspaget HW, Gao Q, Ringers J, Smit VT, Lamers CB, et al. Assessment of serum matrix metalloproteinases MMP-2 and MMP-9 after human liver transplantation: increased serum MMP-9 level in acute rejection. Transplantation. 2004;77(11):1646–52.
Wong W, DeVito J, Nguyen H, Sarracino D, Porcheray F, Dargon I, et al. Chronic humoral rejection of human kidney allografts is associated with MMP-2 accumulation in podocytes and its release in the urine. Am J Transplant Off J Am Soc Transplant Am Soc Transplant Surg. 2010;10(11):2463–71.
de Menezes Neves PD, Machado JR, dos Reis MA, Faleiros AC, de Lima Pereira SA, Rodrigues DB. Distinct expression of interleukin 17, tumor necrosis factor alpha, transforming growth factor beta, and forkhead box P3 in acute rejection after kidney transplantation. Ann Diagn Pathol. 2013;17(1):75–9.
Guan Q, Li S, Gao S, Chen H, Nguan CY, Du C. Reduction of chronic rejection of renal allografts by anti-transforming growth factor-beta antibody therapy in a rat model. American journal of physiology Renal physiology. 2013;305(2):F199–207.
Benza RL, Coffey CS, Pekarek DM, Barchue JP, Tallaj JA, Passineau MJ, et al. Transforming growth factor-beta polymorphisms and cardiac allograft rejection. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 2009;28(10):1057–62.
Burkhardt K, Bosnecker A, Gawaz M, Hillebrand G, Schneeberger H, Schleibner S, et al. Thrombospondin and the expression of adhesion molecules in acute and chronic renal transplant rejection. Transplant Proc. 1993;25(1 Pt 2):1364–5.
Lario S, Bescos M, Campos B, Mur C, Luque P, Alvarez R, et al. Thrombospondin-1 mRNA expression in experimental kidney transplantation with heart-beating and non-heart-beating donors. Journal of nephrology. 2007;20(5):588–95.
Winton HL, Bidwell JL, Armitage WJ. Thrombospondin-1 polymorphisms influence risk of corneal allograft rejection. Invest Ophthalmol Vis Sci. 2014;55(4):2115–20.
Yan Q, Sui W, Wang B, Zou H, Zou G, Luo H. Expression of MMP-2 and TIMP-1 in renal tissue of patients with chronic active antibody-mediated renal graft rejection. Diagn Pathol. 2012;7:141.
The authors thank Ms. Xueping Fan for her invaluable technical support.
This study was undertaken at the Institute of Clinical Science, Zhongshan Hospital, Fudan University.
This work was supported by research grants from the Science and Technology Commission of Shanghai Municipality (10PJ1403600, 18ZR1407200), Shanghai Municipal Commission of Health and Family Planning (201840351), Science and Technology Commission of Qingpu District (QKY2017–03), and the National Natural Science Foundation of China (81470282 and 81870098).
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The current study was approved by the Animal Care and Use Committee (ACUC) of Zhongshan hospital, Fudan University.
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