International Journal of Medical Sciences

Impact factor
2.284

23 October 2018

ISSN 1449-1907 News feeds of published articles

Manuscript login | Account

open access Global reach, higher impact

Journal of Genomics in PubMed Central. Submit manuscript now...

Theranostics

Journal of Cancer

International Journal of Biological Sciences

Journal of Genomics

Journal of Bone and Joint Infection (JBJI)

Oncomedicine

Journal of Biomedicine

Nanotheranostics

PubMed Central Indexed in Journal Impact Factor

Int J Med Sci 2018; 15(9):892-899. doi:10.7150/ijms.24042

Research Paper

A high frequency of CD8+CD28- T-suppressor cells contributes to maintaining stable graft function and reducing immunosuppressant dosage after liver transplantation

Lei Geng1,2,3,*, Jingfeng Liu1,2,3,*, Junjie Huang1,2,3, Bingyi Lin1,2,3, Songfeng Yu1,2,3, Tian Shen1,2,3, Zhuoyi Wang1,2,3, Zhe Yang1,2,3, Lin Zhou1,2,3, Shuseng Zheng1,2,3, Corresponding address

1. Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, The First Affiliated Hospital, Zhejiang University, Hangzhou 310003, China
2. Division of Liver Transplantation, Key Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, The First Affiliated Hospital, Zhejiang University, Hangzhou 310003, China
3. Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou 310003, China
*These authors contribute equally to the study.

This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
How to cite this article:
Geng L, Liu J, Huang J, Lin B, Yu S, Shen T, Wang Z, Yang Z, Zhou L, Zheng S. A high frequency of CD8+CD28- T-suppressor cells contributes to maintaining stable graft function and reducing immunosuppressant dosage after liver transplantation. Int J Med Sci 2018; 15(9):892-899. doi:10.7150/ijms.24042. Available from http://www.medsci.org/v15p0892.htm

Abstract

CD8+CD28-T cells (CD8Ts) exert immunosuppressive effects in various autoimmune diseases. The current study was designed to investigate the role of defects in CD8Ts in liver transplantation (LT). The proportion of CD8Ts in peripheral blood was determined by flow cytometry. The mean proportion of CD8Ts was 23.39% in recipients with stable graft function and 16.64% in those with graft dysfunction following LT compared with 19.86% in the healthy cohort. After receiving enhanced immunosuppressive therapy, patients in the rejection group who achieved recovery of graft function showed an increase in the proportion of CD8Ts (from 17.39% to 25.55%), but those in the group with refractory graft dysfunction showed no significant change (12.49% to 10.30%). Furthermore, in the first year after LT, recipients longer removed in time from the LT date exhibited a higher proportion of CD8Ts. Patients benefited most from tacrolimus concentrations of 5-10 ng/ml in the first year after LT and 0-5 ng/ml thereafter. Moreover, the change in the proportion of CD8Ts (ΔCD8Ts) was significantly higher in recipients with stable graft function than in those with graft dysfunction. These results suggest that a high frequency of CD8Ts prevents rejection and contributes to reduce immunosuppressant dosage and even induces tolerance.

Keywords: CD8+CD28-T cells, Liver transplantation, Tacrolimus, Rejection

Introduction

The burden of hepatitis B virus infection is heaviest in China, where approximately 20 million individuals have chronic hepatitis B and about five million patients eventually progress to irreversibly decompensated liver cirrhosis or hepatocellular carcinoma (HCC)(1). Liver transplantation (LT) is considered the best life-saving therapy for patients with end-stage liver disease. In recent decades, the development and broad administration of immunosuppressive drugs has contributed to increased graft survival rates(2). However, although rejection is commonly mild for LT compared with that for other solid organs, life-long immunosuppressive therapy is still required(3). Accumulating evidence has confirmed that adverse effects such as chronic kidney dysfunction, recurrent and de novo malignancy, infections, and cardiovascular events have become the dominant concerns associated with long-term administration of immunosuppressants, particularly calcineurin inhibitors (CNIs)(4). Undoubtedly, a minimum immunosuppressant strategy or complete withdrawal is beneficial for improving long-term survival rate and quality of life for recipients after LT(5).

Prospective multicenter clinical trials have shown that immunosuppressive drugs could be completely withdrawn for up to 20% of recipients with LT(6, 7). A comparison with recipients who showed failure of immunosuppressant withdrawal suggested that an increased proportion of regulatory T (Treg) cells is a crucial distinguishing immune characteristic(8). In one study, Okumura et al. transferred enriched, ex vivo-expanded regulatory T-cell into 10 consecutive adult recipients early post-LT. At the end of the pilot study, these candidates were immunosuppressant free for more than 1 year, revealing that regulatory T-cell-based cell therapy was safe and effective for drug minimization and induction of operational tolerance in LT(9). Activation, expansion and differentiation of effective primary T cells in allograft rejection is dependent on CD28-mediated co-stimulation(10). Loss of the CD28 co-stimulation signal results in a CD8-positive T-cell-mediated immunosuppressive effect through decreased expression of the co-stimulatory molecules CD40, CD80, and CD86 in CD4+ T helper cells(11), increasing expression of the inhibitory receptors ILT3 and ILT4 in antigen-presenting cells (APCs)(12-14). It also increases secretion of inhibitory cytokines such as IL10 and TGFβ by cells commonly referred to as CD8+CD28- T suppressor cells (CD8Ts)(15).

The role of defective CD8Ts in autoimmune diseases and rejection following organ transplantation has recently been confirmed, an observation that has attracted considerable attention(16). Tulunay et al. reported that a decrease in the CD8Treg population impairs T cell suppression and increases the population of autoreactive B cells, resulting in progression of systemic lupus erythematosus(17). In patients with rheumatoid arthritis, the suppressive function of CD8Ts was found to be deficient, as evidenced by decreased co-stimulator expression and increased expression of PDCD1 (programmed cell death 1)(18). Furthermore, expansion of CD8Ts has been shown to decrease the need for immunosuppressant maintenance and to contribute to preventing acute and chronic rejection and sustaining normal graft function after heart-kidney transplantation(19). However, there is little information available on the clinical significance of CD8Ts, and the factors that contribute to the expansion of CD8Ts after LT are still unknown. Accordingly, this study was designed to explore the protective role of CD8Ts in maintaining graft function and assess the relationship between CD8Ts and immunosuppressant administration following LT.

Material and Methods

Ethics statement

The study was performed in accordance with the ethics guidelines of the 1975 Declaration of Helsinki and with the consent of the Ethics Committee of Zhejiang University. All patients provided informed written consent.

Study objectives and data collection

Venous blood samples were obtained from 280 adult recipients of a liver transplant. Donor livers were obtained from deceased cardiac failure patients or their living family members. Eligibility for LT followed HangZhou criteria for HCC candidates and standard King's College Hospital criteria for candidates with acute or chronic acute liver failure. Recipient demographics, pre-transplant therapies, operative variables, and pathological characteristics were prospectively obtained from the LT database at the First Affiliated Hospital of Zhejiang University through the hospital information collection system.

Recipient management and surveillance after LT

The post-transplantation immunosuppression protocol consisted of tacrolimus, basiliximab, corticosteroids, and mycophenolate mofetil. The target tacrolimus concentration range was 10-15 ng/mL during the first month, and was subsequently titrated down to the minimum concentration required to maintain long-term stable graft function. Methylprednisolone was initiated at a daily dose of 1000 mg in the perioperative phase, and was gradually tapered and withdrawn during the first month after LT. Mycophenolate mofetil was administered at a fixed dose of 500 mg twice daily after LT. Basiliximab was administrated twice, on post-transplantation days 1 and 4.

Recipients were followed closely via a communication system and the outpatient service from the date of hospital discharge to the last follow-up visit. Blood tacrolimus was routinely monitored before daily tacrolimus administration using the PRO-Trac TMII Tacrolimus Elisa Kit (Diasorin, Stillwater, MN, USA) according to the manufacturer's instructions. Biochemical tests, ultrasonography, emission computed tomography, and liver puncture were utilized to monitor graft function.

Flow cytometry analysis

Venous blood samples were divided into two tubes for testing tacrolimus concentration and the proportion of CD8Ts. Peripheral blood mononuclear cells (PBMCs) were isolated and incubated with fluorescein isothiocyanate (FITC)-conjugated anti-CD8 and phycoerythrin (PE)-conjugated anti-CD28 antibodies. Isotype controls were utilized to determine background fluorescence. After washing PBMCs three times with phosphate-buffered saline, CD8 and CD28 expression was determined based on 1 × 105 cellular events using a 4-color FC500 flow cytometer (Beckman-Coulter, Miami, FL, USA).

 Table 1 

Demographics and clinical characteristic of LT recipients

VariablesValue
Age (yr)50.83 ± 10.15
GenderMale196 (74.24%)
Female68 (25.76%)
The time from LT date (mo)30.08 ± 34.89
MELD score17 (range, 8-37)
Child-Pugh score8 (range, 4-15)
EtiologyHBV-related cirrhosis164 (62.12%)
Hepatocellular carcinoma87 (32.95%)
Other13 (4.92%)
Blood testsBilirubin (μmol/L)(NR<17.1)26.73 ± 64.20
AST (IU/L) (NR<50)27.69 ± 62.17
ALT (IU/L) (NR<40)35.41 ± 115.9
Albumin (g/L) (NR 35-50)38.46 ± 5.71
WBC (*109/L)5.14 ± 1.78
Lymphocyte (*109/L)1.40 ± 0.83
Neutrophil (*109/L)2.91 ± 1.59
Urea (μmol/L)(NR3-7.1)4.63 ± 3.28
Creatinine (μmol/L)(NR 60-97)78.52 ± 39.64
Tarcrolimus6.14 ± 2.31
ABOA-A83 (31.44%)
B-B75 (28.41%)
AB-AB49 (18.56%)
O-O57 (21.59%)

NOTE: Date are presented as frequency (percentage) or mean ± SD. NR, Normal range; AST, aspartate aminotransferase; ALT, alanine aminotransferase; WBC, white blood cell; HBV, hepatitis B virus; MELD, Model for End-stage Liver Disease.

 Table 2 

Clinical characteristics of rejection and non-rejection groups

VariablesRejection (n = 26)Non-rejection (n = 238)P-value
Age (SD, yr)48.81 (9.84)51.55 (9.96)0.18
GenderMale191771.00
Female761
The time from LT date (mo)26.34 ± 33.7224.11 ± 35.190.75
Pre-transplant MELD score22.46 ± 11.1520.64 ± 11.180.43
Pre-transplant Child score9.54 ± 2.739.38 ± 2.780.78
Bilirubin (μmol/L)33.46 ± 29.5517.03 ± 14.21<0.01
AST (IU/L)69.42 ± 50.1627.55 ± 16.56<0.01
ALT (IU/L)65.15 ± 52.7324.39 ± 18.75<0.01
Lymphocyte (×109/L)0.98 ± 0.841.40 ± 0.830.015
Tarcrolimus6.84 ± 2.686.13 ± 2.310.14
Total ischemia (min)182 ± 123207 ± 1060.26
CD8T proportion (%)16.64 ± 10.8523.39 ± 11.33<0.01

Statistical analysis

Experimental data are presented as frequencies or means ± standard deviation (SD). Student's t test and Fisher's exact test were used to analyze the correlation between the proportion of CD8Ts and clinico-pathological parameters. SPSS19.0 software (SPSS Inc., Chicago, IL, USA) was utilized for statistical analysis, and a P-value less than 0.05 was considered statistically significant.

Results

Patient demographics and outcomes

The demographics and pre-transplant diseases of recipients are presented in Table 1. Subjects who had received ABO-incompatible transplants (n=22), kidney-liver transplants (n=1), or a second LT (n=3) were excluded from the study. Of the 264 adult patients enrolled in the study, 196 (74.2%) were men and 68 (25.8%) were women. The mean age of recipients was 50.83±10.15 years at transplantation. Pre-LT diagnoses included HCC and chronic liver failure. The mean MELD (Model for End-Stage Liver Disease) score was 17, the mean Child Turcotte Pugh score was 8, and total ischemia time was 254 min.

Except for patients with rejection, recipients were divided based on long-term maintenance tacrolimus concentrations into a 0-5 ng/ml group, a 5-10 ng/ml group, and a >10 ng/ml group. Of the 26 recipients with graft dysfunction, four were confirmed as acute rejection, and the remaining patients were considered chronic rejection. After receiving enhanced immunosuppressant therapy, 15 of these recipients recovered graft function, whereas 11 did not.

A high proportion of CD8Ts supports maintenance of normal graft function and reduces immunosuppressant dosage requirements

The demographics and clinical characteristics of both rejection and non-rejection groups are presented in Table 2. Compared with patients without graft dysfunction, patients with graft dysfunction exhibited a significantly reduced proportion of CD8Ts (Figure 1A-C). Specifically, the proportion of CD8Ts was 23.39% in the non-rejection group, 19.86% in the healthy cohort, and only 16.64% in the rejection group (Figure 1D). Furthermore, the proportion of CD8Ts increased from 17.39% to 25.55% in patients who achieved recovery of graft function after receiving enhanced immunosuppressive therapy (Figure 1E). However, in the patient population with refractory graft dysfunction, the CD8T proportion did not increase and was even decreased in some patients, averaging 12.49% before receiving enhanced immunosuppressive therapy and 10.30% after therapy (Figure 1F). In addition, there was no significant difference in tacrolimus concentration between recipients with a high and low proportion of CD8Ts during long-term maintenance. However, 10 recipients in the group with a high proportion of CD8Ts, but only 1 patient in the low-CD8T proportion group, received 0-5 ng/ml tacrolimus for maintenance of graft function (Table 3). Notably, nine recipients whose immunosuppressants were successfully withdrawn exhibited a high proportion of CD8Ts (Figure 1D). These results suggest that a high proportion of CD8Ts contributes to maintaining normal graft function and reducing immunosuppressant requirements.

 Figure 1 

(A-C) The proportion of CD8Ts in a recipient without graft dysfunction (A), a patient with graft dysfunction (B), and a recipient with immunosuppressant withdrawal (C). (D) Summary data showing the proportion of CD8Ts among groups. (E) CD8T proportions in relation to recovery of graft function in recipients with rejection. (F) CD8T proportions in patients with refractory graft dysfunction.

Int J Med Sci Image (Click on the image to enlarge.)
 Table 3 

Characteristics of 10 recipients with immunosuppressant withdrawal

VariablesValue
Age at LT (yr)45.21 ± 8.72 (range, 27-56)
Gender (female:male)2:8 (20%:80%)
Etiology of liver disease
Fulminant hepatitis1 (10%)
Virus hepatitis B related cirrhosis3 (30%)
HCC6 (60%)
Rejection history1 (10%)
Tacrolimus levels
Time from LT date (years)4.56
Graft type
LDLT1 (10%)
DCDLT9 (90%)
Meld score22.56 ± 7.45 (range, 21-28)
Child-Pugh score9 (5-14)
CD8+ T cell proportion (%)31.67 (21.22-45.63)

Relationship between the proportion of CD8Ts and clinico-pathological parameters

Accumulating evidence has revealed that age and immunosuppressants are two important determinants of Treg cell proportions(20, 21). In the current study, recipients 70 years and older with 0-5 ng/ml tacrolimus exhibited lower proportions of CD8Ts compared with other age groups (Figure 2A). Excluding 70 years and older patients, the median proportion of CD8Ts was 26.46% in the >10 ng/ml tacrolimus group, 21.24% in the 5-10 ng/ml tacrolimus group, and 17.32% in the 0-5 ng/ml tacrolimus group (Figure 2B). The long-term presence of alloantigens potentially impairs the immune response and induces immune tolerance. Therefore, we tested whether the time from transplant date affected the proportion of CD8Ts. After adjusting for age and tacrolimus concentration, in the first year, recipients longer removed from the transplant date exhibited a higher proportion of CD8Ts (Figure 2C). Furthermore, in the first year after LT, the proportion of CD8Ts was higher in the >5 ng/ml tacrolimus group than in the 0-5 ng/ml tacrolimus group. However, beyond one year after LT, the CD8T proportion-increasing effect of tacrolimus was lost (Figure 2D).

 Figure 2 

(A) The proportion of CD8Ts in recipients as function of age. (B) The proportion of CD8Ts in patients in >10, 5-10, and 0-5 ng/ml tacrolimus groups. (C, D) Proportion of CD8Ts in patients during the first year after LT (C) and at later time points (D).

Int J Med Sci Image (Click on the image to enlarge.)
 Figure 3 

(A, B) The number of lymphocytes (A) and absolute value of CD8Ts (B) in graft-dysfunction and normal graft function groups. There were no significant differences between groups. (C, D) Median proportion of CD8+CD28+ T cells (C) and ΔCD8T proportion (D) in the normal function group and graft-dysfunction group.

Int J Med Sci Image (Click on the image to enlarge.)

The proportion of CD8Ts is more important than the absolute number of CD8Ts

There was no significant difference in lymphocyte numbers between the graft-dysfunction group and the normal graft function group, but lymphocytopenia was less frequent in the patient population with rejection (Figure 3A). Although the proportion of CD8Ts was lower in the graft-dysfunction group, the absolute number of CD8Ts was not different between the two groups (Figure 3B). These results indicate that the proportion of CD8Ts is more important than their absolute numbers for maintenance of graft function.

The change in the proportion of CD8Ts (ΔCD8Ts) predicts graft function

We further found that the proportion of CD8+CD28+ T cells was not different between recipients with stable graft function and those with graft dysfunction (Figure 3C). Interestingly, the ΔCD8T proportion (proportion of CD8Ts minus the proportion of CD8+CD28+ T cells) was higher in the stable graft function group than in the graft-dysfunction group (Figure 3D). In addition, only two recipients with stable graft function exhibited lower proportions of CD8Ts than CD8+CD28+ T cells, but more than half of recipients with graft dysfunction showed a lower proportion of CD8Ts. These results suggest that the ΔCD8T proportion is a precise predictor of graft function following LT.

Discussion

Although the liver exhibits immune privilege compared with other organs, the rate of acute rejection was still as high as 15.6% from 2005-2013 in the USA according to data from the Science Registry of Transplant Recipients(22). Furthermore, given the seriously limited availability of donor livers compared with organ demand, several transplant centers have expanded the criteria of donors to include donors older than 60 years of age, and those with macrovesicular steatosis ≥ 30%, hot ischemia time > 40 minutes, cold ischemia time > 10 hours, and moderate liver dysfunction(23, 24). The utilization of extended criteria for donor grafts has undoubtedly contributed to the frequency of rejection, which, in turn, significantly increases the hazard ratio for graft failure and death after LT(22). Therefore, powerful immunosuppressive therapy remains necessary, especially during the early time following LT. However, the need to decrease immunosuppressant-related death while preventing rejection presents a conundrum. Abundant evidence has confirmed that a high proportion of immunosuppressive cells, including CD4-positive regulatory T cells and tolerant dendritic cells, reduces the dosage of immunosuppressant required while also decreasing the rate of rejection(9).

CD8Ts have recently been recognized as an important Treg cell subset whose dysfunction and deficiency are involved in the development of various autoimmune diseases(16, 17). The co-stimulatory signal provided by CD28 is important for effective expansion of primary T cells(25) and development of graft-versus-host disease and rejection(26, 27). Blocking CD28 results in graft acceptance and activation of CD4+ Treg cells(10, 28). It has been reported that CD8Ts are present in LT recipients(29), but little is known about the relationship between CD8Ts and clinical characteristics. In the current study, we analyzed the proportion of CD8Ts and collected information from 264 LT patients. We found that the proportion of CD8Ts was significantly lower in the graft-dysfunction group than in the stable graft function group. In addition, most recipients that recovered from graft dysfunction exhibited an increase in the proportion of CD8Ts after receiving enhanced immunosuppressive therapy, but those without recovery showed no such increase. Moreover, a higher proportion of CD8Ts was found in recipients with recovery of graft function than in those without recovery. These findings indicate that CD8Ts are crucial for maintaining the stability of graft function.

Similar to the effect of CD4+ Treg cells on immunosuppression, the high proportion of CD8Ts has been confirmed to reduce the maintenance dose of immunosuppressants in recipients with cadaveric heart-kidney transplants or pediatric liver-intestine transplants(19, 30). However, in the LT cohort, we found that the proportion of CD8Ts was higher in recipients with a higher tacrolimus concentration. The mean proportion of CD8Ts in recipients with 0-5 ng/ml tacrolimus approached that of the rejection group, but was higher, and apparently sufficient to maintain stable graft function, in the 5-10 ng/ml and >10 ng/ml tacrolimus groups. Furthermore, within 1 year from the time of LT date, longer post-LT times were associated with a higher proportion of CD8Ts, but this relationship did not hold beyond 1 year. Interestingly, the effect of tacrolimus on the proportion of CD8Ts was only evident within the first year after LT. These results suggest that LT patients should be administered 5-10 ng/ml tacrolimus in the first year after LT and maintained with 0-5 ng/ml tacrolimus thereafter. In other words, the proportion of CD8Ts could be used as a precise indicator of graft function and inform decisions regarding reducing the dose of immunosuppressant administered. Importantly, we further found that immunosuppressant could be completely withdrawn after LT in 10 recipients with a proportion of CD8Ts > 30%.

These findings highlight the importance of knowing how to induce and expand CD8Ts. As early as 1998, Suciu-Foca et al. confirmed that CD8Ts achieve suppression by specifically recognizing the MHC class I antigens expressed by APCs and inhibiting B7 expression in APCs(11). This group subsequently demonstrated the successful induction of CD8Ts in vitro through immunization with human PBMCs(31). Furthermore, using a second-generation CTLA-4-immunoglobulin fusion protein, Guinan et al. showed that blocking CD28-mediated co-stimulation resulted in approximately an 8-fold expansion of CD8Ts(32). A study of CD4-depleted T-cell lines further suggested that proliferation of CD8Ts requires exogenous interleukin-2(33). Unfortunately, despite considerable advances in CD8T induction methods, transfusion of CD8Ts expanded in vitro as an immunosuppressive therapy has not yet proved successful. Finally, the current study also confirmed that the proportion of CD8Ts is more important than the absolute number of CD8Ts in maintaining stable graft function, and the ΔCD8T proportion could be a precise predictor for monitoring graft function.

Conclusions

The proportion of CD8Ts is significantly decreased in recipients with graft dysfunction compared with those with stable graft function. Age, time from transplant date, and immunosuppressants are the main factors that influence the proportion of CD8Ts. Furthermore, the proportion of CD8Ts and the ΔCD8T proportion are sensitive predictors of graft function.

Acknowledgements

This work was supported by grants from the Zhejiang Provincial Natural Science Foundation of China (LY18H030002, LY14H030003, LQ13H160004, LY15H160016, LQ15H030003), the National Natural Science Foundation of China (81302074, 81373160, 81400673), Fundamental Research Funds for the Central Universities (2017FZA7009) and the Medical and Health Plan of Zhejiang Province (201472813).

Competing Interests

The authors have declared that no competing interest exists.

References

1. Chen W, Zheng R, Baade PD, Zhang S, Zeng H, Bray F, Jemal A. et al. Cancer statistics in China, 2015. CA Cancer J Clin. 2016;66:115-132

2. A comparison of tacrolimus (FK 506) and cyclosporine for immunosuppression in liver transplantation. The U.S. Multicenter FK506 Liver Study Group. N Engl J Med. 1994;331:1110-1115

3. Adam R, McMaster P, O'Grady JG, Castaing D, Klempnauer JL, Jamieson N, Neuhaus P. et al. Evolution of liver transplantation in Europe: report of the European Liver Transplant Registry. Liver Transpl. 2003;9:1231-1243

4. Wiesner RH, Fung JJ. Present state of immunosuppressive therapy in liver transplant recipients. Liver Transpl. 2011;17(Suppl 3):S1-9

5. Jia JJ, Lin BY, He JJ, Geng L, Kadel D, Wang L, Yu DD. et al. ''Minimizing tacrolimus'' strategy and long-term survival after liver transplantation. World J Gastroenterol. 2014;20:11363-11369

6. Benitez C, Londono MC, Miquel R, Manzia TM, Abraldes JG, Lozano JJ, Martinez-Llordella M. et al. Prospective multicenter clinical trial of immunosuppressive drug withdrawal in stable adult liver transplant recipients. Hepatology. 2013;58:1824-1835

7. Orlando G, Soker S, Wood K. Operational tolerance after liver transplantation. J Hepatol. 2009;50:1247-1257

8. Martinez-Llordella M, Puig-Pey I, Orlando G, Ramoni M, Tisone G, Rimola A, Lerut J. et al. Multiparameter immune profiling of operational tolerance in liver transplantation. Am J Transplant. 2007;7:309-319

9. Todo S, Yamashita K, Goto R, Zaitsu M, Nagatsu A, Oura T, Watanabe M. et al. A pilot study of operational tolerance with a regulatory T-cell-based cell therapy in living donor liver transplantation. Hepatology. 2016;64:632-643

10. Hunig T, Luhder F, Elflein K, Gogishvili T, Frohlich M, Guler R, Cutler A. et al. CD28 and IL-4: two heavyweights controlling the balance between immunity and inflammation. Med Microbiol Immunol. 2010;199:239-246

11. Liu Z, Tugulea S, Cortesini R, Suciu-Foca N. Specific suppression of T helper alloreactivity by allo-MHC class I-restricted CD8+CD28- T cells. Int Immunol. 1998;10:775-783

12. Manavalan JS, Kim-Schulze S, Scotto L, Naiyer AJ, Vlad G, Colombo PC, Marboe C. et al. Alloantigen specific CD8+CD28- FOXP3+ T suppressor cells induce ILT3+ ILT4+ tolerogenic endothelial cells, inhibiting alloreactivity. Int Immunol. 2004;16:1055-1068

13. Chang CC, Ciubotariu R, Manavalan JS, Yuan J, Colovai AI, Piazza F, Lederman S. et al. Tolerization of dendritic cells by T(S) cells: the crucial role of inhibitory receptors ILT3 and ILT4. Nat Immunol. 2002;3:237-243

14. Cortesini R, Suciu-Foca N. ILT3+ ILT4+ tolerogenic endothelial cells in transplantation. Transplantation. 2006;82:S30-32

15. Liu Q, Zheng H, Chen X, Peng Y, Huang W, Li X, Li G. et al. Human mesenchymal stromal cells enhance the immunomodulatory function of CD8(+)CD28(-) regulatory T cells. Cell Mol Immunol. 2015;12:708-718

16. Filaci G, Fenoglio D, Indiveri F. CD8(+) T regulatory/suppressor cells and their relationships with autoreactivity and autoimmunity. Autoimmunity. 2011;44:51-57

17. Tulunay A, Yavuz S, Direskeneli H, Eksioglu-Demiralp E. CD8+CD28-, suppressive T cells in systemic lupus erythematosus. Lupus. 2008;17:630-637

18. Ceeraz S, Hall C, Choy EH, Spencer J, Corrigall VM. Defective CD8+CD28+ regulatory T cell suppressor function in rheumatoid arthritis is restored by tumour necrosis factor inhibitor therapy. Clin Exp Immunol. 2013;174:18-26

19. Colovai AI, Mirza M, Vlad G, Wang S, Ho E, Cortesini R, Suciu-Foca N. Regulatory CD8+CD28- T cells in heart transplant recipients. Hum Immunol. 2003;64:31-37

20. Pantaleo G, Demarest JF, Soudeyns H, Graziosi C, Denis F, Adelsberger JW, Borrow P. et al. Major expansion of CD8+ T cells with a predominant V beta usage during the primary immune response to HIV. Nature. 1994;370:463-467

21. Furukawa A, Wisel SA, Tang Q. Impact of Immune-Modulatory Drugs on Regulatory T Cell. Transplantation. 2016;100:2288-2300

22. Levitsky J, Goldberg D, Smith AR, Mansfield SA, Gillespie BW, Merion RM, Lok AS. et al. Acute Rejection Increases Risk of Graft Failure and Death in Recent Liver Transplant Recipients. Clin Gastroenterol Hepatol. 2016

23. Cameron AM, Ghobrial RM, Yersiz H, Farmer DG, Lipshutz GS, Gordon SA, Zimmerman M. et al. Optimal utilization of donor grafts with extended criteria: a single-center experience in over 1000 liver transplants. Ann Surg. 2006;243:748-753 discussion 753-745

24. Briceno J, Ciria R, de la Mata M, Rufian S, Lopez-Cillero P. Prediction of graft dysfunction based on extended criteria donors in the model for end-stage liver disease score era. Transplantation. 2010;90:530-539

25. Nielsen KN, Steffensen MA, Christensen JP, Thomsen AR. Priming of CD8 T cells by adenoviral vectors is critically dependent on B7 and dendritic cells but only partially dependent on CD28 ligation on CD8 T cells. J Immunol. 2014;193:1223-1232

26. Luo Y, Liang F, Liu N, Xue H, Song X, Yuan F, Long J. et al. Potent control of acute graft-versus-host disease lethality after immunization with a novel DNA vaccine targeted to B7-1/CD28 costimulatory signaling pathway. J Immunother. 2013;36:82-92

27. Nakatsuji T. Better-surviving liver grafts by the injection of anti-CD2 antibody: the important roles of host CD8+ and CD2+CD28+ T cells in chronic graft rejection and beta type platelet-derived growth factor receptor (PDGFR-beta) expression on apoptotic liver grafts. Tohoku J Exp Med. 1999;187:215-225

28. Lehnert AM, Mottram PL, Han W, Walters SN, Patel AT, Hawthorne WJ, Cowan PJ. et al. Blockade of the CD28 and CD40 pathways result in the acceptance of pig and rat islet xenografts but not rat cardiac grafts in mice. Transpl Immunol. 2001;9:51-56

29. Lin YX, Wang LL, Yan LN, Cai P, Li B, Wen TF, Zeng Y. Analysis of CD8+CD28- T-suppressor cells in living donor liver transplant recipients. Hepatobiliary Pancreat Dis Int. 2009;8:241-246

30. Sindhi R, Manavalan JS, Magill A, Suciu-Foca N, Zeevi A. Reduced immunosuppression in pediatric liver-intestine transplant recipients with CD8+CD28- T-suppressor cells. Hum Immunol. 2005;66:252-257

31. Jiang S, Tugulea S, Pennesi G, Liu Z, Mulder A, Lederman S, Harris P. et al. Induction of MHC-class I restricted human suppressor T cells by peptide priming in vitro. Hum Immunol. 1998;59:690-699

32. Barbon CM, Davies JK, Voskertchian A, Kelner RH, Brennan LL, Nadler LM, Guinan EC. Alloanergization of human T cells results in expansion of alloantigen-specific CD8(+) CD28(-) suppressor cells. Am J Transplant. 2014;14:305-318

33. Colovai AI, Liu Z, Ciubotariu R, Lederman S, Cortesini R, Suciu-Foca N. Induction of xenoreactive CD4+ T-cell anergy by suppressor CD8+CD28- T cells. Transplantation. 2000;69:1304-1310

Author contact

Corresponding address Corresponding author: Shusen Zheng, Email: ShusenZhengedu.cn, Address: Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, The First Affiliated Hospital, College of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou 310003, China. Tel: +8657187236601; Fax: +8657187236628


Received 2017-11-27
Accepted 2018-2-27
Published 2018-6-4