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Immunology and Infection

New Tools to Expand Regulatory T Cells from HIV-1-infected Individuals

Published: May 30th, 2013

DOI:

10.3791/50244

1Ragon Institute of MGH, MIT, and Harvard, 2Division of Infectious Diseases, Massachusetts General Hospital

CD4+ Regulatory T cells are potent immune-modulators and serve important functions in immune homeostasis. The paucity of these cells in peripheral blood makes functional studies challenging, specifically in the context of HIV-1-infection. We here describe a method to isolate and expand functional CD4+ Tregs from peripheral blood from HIV-1-infected individuals.

CD4+ Regulatory T cells (Tregs) are potent immune modulators and serve an important function in human immune homeostasis. Depletion of Tregs has led to measurable increases in antigen-specific T cell responses in vaccine settings for cancer and infectious pathogens. However, their role in HIV-1 immuno-pathogenesis remains controversial, as they could either serve to suppress deleterious HIV-1-associated immune activation and thus slow HIV-1 disease progression or alternatively suppress HIV-1-specific immunity and thereby promote virus spread. Understanding and modulating Treg function in the context of HIV-1 could lead to potential new strategies for immunotherapy or HIV vaccines. However, important open questions remain on their role in the context of HIV-1 infection, which needs to be carefully studied.

Representing roughly 5% of human CD4+ T cells in the peripheral blood, studying the Treg population has proven to be difficult, especially in HIV-1 infected individuals where HIV-1-associated CD4 T cell and with that Treg depletion occurs. The characterization of regulatory T cells in individuals with advanced HIV-1 disease or tissue samples, for which only very small biological samples can be obtained, is therefore extremely challenging. We propose a technical solution to overcome these limitations using isolation and expansion of Tregs from HIV-1-positive individuals.

Here we describe an easy and robust method to successfully expand Tregs isolated from HIV-1-infected individuals in vitro. Flow-sorted CD3+CD4+CD25+CD127low Tregs were stimulated with anti-CD3/anti-CD28 coated beads and cultured in the presence of IL-2. The expanded Tregs expressed high levels of FOXP3, CTLA4 and HELIOS compared to conventional T cells and were shown to be highly suppressive. Easier access to large numbers of Tregs will allow researchers to address important questions concerning their role in HIV-1 immunopathogenesis. We believe answering these questions may provide useful insight for the development of an effective HIV-1 vaccine.

With more than 34 million individuals living with HIV/AIDS worldwide and an estimated 2.5 million people newly infected in 2011, the need for an effective HIV vaccine to curb the worldwide HIV epidemic remains paramount. However, despite three decades of intense research efforts, the HIV-1 vaccine efficacy trials to date have resulted in only modest protection 1-3 and the correlates of protective immunity remain poorly understood. Elucidating the nature of the immune response needed for protection is essential for the strategic design of an effective HIV-1 vaccine and other immunotherapeutic strategies targeting HIV-1 infection.

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1. Regulatory T cell isolation from HIV-1 Positive Blood

  1. Carefully transfer blood, collected in ACD tubes, into a 50 ml conical tube for a final volume of 15 ml blood per tube.
  2. Add 25 μl/ml of blood of RosetteSep Human CD4+ T Cell Enrichment Cocktail, mix carefully and incubate 20 min at room temperature.
  3. Add 15 ml of PBS/2% FBS to the blood and mix carefully. Layer the diluted blood sample on top of 15 ml of Histopaque at room temperature in a 50 ml conical tube. Spin the conical t.......

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The expression of interleukin 2 receptor (CD25) and the interleukin 7 receptor (CD127) have been described as reliable surface markers to identify functional Treg populations 13 and have been shown to correlate with CD4+CD25+FOXP3+ Tregs 9,12. Figure 1 represents the gating strategy used to flow-sort single CD3+CD4+CD25+CD127low Tregs from PBMC isolated from an HIV-1-positive individual. The CD25/CD127 anti.......

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Using the protocol described above, Tregs can be successfully isolated and expanded from HIV-1-infected individuals in vitro. Expanded Tregs express high levels of FOXP3, CTLA4 and HELIOS, are highly suppressive and display a highly demethylated Treg-Specific Demethylation Region (TSDR) locus of the FOXP3 gene (data not shown) 15, suggesting true origin from the regulatory T cell lineage, as opposed to activation-induced transient FOXP3 upregulation. Deep sequencing demonstrated that the TCR repertoir.......

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This work was supported in part by research funding from the Elisabeth Glaser Pediatric AIDS Foundation (Pediatric HIV Vaccine Program Award MV-00-9-900-1429-0-00 to MMA), MGH/ECOR (Physician Scientist Development Award to MMA), NIH NIAID (KO8219 AI074405 and AI074405-03S1 to MMA), and the Harvard University Center for AIDS Research (CFAR), an NIH funded program (P30 AI060354) which is supported by the following NIH Co-Funding and Participating Institutes and Centers: NIAID, NCI, NICHD, NHLBI, NIDA, NIMH, NIA, FIC, and OAR. These studies were furthermore supported by the Bill & Melinda Gates Foundation and the Terry and Susan Ragon Foundation.

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Name Company Catalog Number Comments
      Reagents
RosetteSep Human CD4+ T Cell Enrichment Cocktail Stemcells technologies 15062  
PBS Sigma D8537  
FBS Sigma F4135  
Histopaque Sigma H8889  
Anti-CD3-PECy7 BD Pharmingen 557851  
Anti-CD4-FITC eBioscience 11-0049-42  
Anti-CD25-APC eBioscience 17-0259-42  
Anti-CD127-PE BD Pharmingen 557938  
Round-Bottom tube with 35 μm a nylon mesh BD Falcon 352235  
X-VIVO 15 Lonza 04-418Q  
Penicillin/Streptomycin Mediatech 30-001-Cl  
Human Serum Gemini Bio-Products 100-512  
Human T-activator CD3/CD28 Life Technologies 111.31D  
IL-2 NIH Aids Research & Reference Reagent Program 136  
LIVE/DEAD Fixable Violet Dead Cell Stain Kit Life technologies L34955  
Anti-CD4-qdot-655 Life Technologies Q10007  
Anti-CD25-PECy5 eBiosciences 15-0259-42  
Foxp3 / Transcription Factor Staining Buffer Set eBiosciences 00-5523-00  
Anti-FOXP3-PE eBiosciences 12-4776-42  
Anti-HELIOS-FITC Biolegend 137204  
Anti-CTLA4-APC BD Pharmingen 555855  
CellTrace Violet Cell Proliferation Kit Life Technologies C34557  
Vybrant CFDA SE Cell Tracer Kit Life Technologies V12883  
HEPES Mediatech 25-060-Cl  
Treg Suppression inspector Miltenyi Biotec 130-092-909  
Anti-CD4-APC BD Pharmingen 340443  
Anti-CD8-AF700 BD Pharmingen 557945  
RPMI 1640 Sigma R0883  
Glutamine Mediatech 25-002-Cl  
      Materials
BD Vacutainer Blood Collection Tube w/ ACID CITRATE DEXTROSE (ACD) Becton, Dickinson and Company (BD) 364606  
FACSAria IIu Cell Sorter BD Biosciences -  
LSR II Flow Cytometer BD Biosciences -  
FlowJo Tree Star v887  

  1. Rerks-Ngarm, S., et al. Vaccination with ALVAC and AIDSVAX to prevent HIV-1 infection in Thailand. N. Engl. J. Med. 361, 2209-2220 (2009).
  2. Buchbinder, S. P., et al. Efficacy assessment of a cell-mediated immunity HIV-1 vaccine (the Step Study): a double-blind, randomised, placebo-controlled, test-of-concept trial. Lancet. 372 (08), 1881-1893 (2008).
  3. Pitisuttithum, P., et al. Randomized, double-blind, placebo-controlled efficacy trial of a bivalent recombinant glycoprotein 120 HIV-1 vaccine among injection drug users in Bangkok, Thailand. J. Infect. Dis. 194, 1661-1671 (2006).
  4. Morse, M. A., et al. Depletion of human regulatory T cells specifically enhances antigen-specific immune responses to cancer vaccines. Blood. 112, 610-618 (2008).
  5. Furuichi, Y., et al. Depletion of CD25+CD4+T cells (Tregs) enhances the HBV-specific CD8+ T cell response primed by DNA immunization. World J. Gastroenterol. 11, 3772-3777 (2005).
  6. Rech, A. J., Vonderheide, R. H. Clinical use of anti-CD25 antibody daclizumab to enhance immune responses to tumor antigen vaccination by targeting regulatory T cells. Ann. N.Y. Acad. Sci. 1174, 99-106 (2009).
  7. Ruter, J., et al. Altering regulatory T cell function in cancer immunotherapy: a novel means to boost the efficacy of cancer vaccines. Front Biosci. 14, 1761-1770 (2009).
  8. Moreno-Fernandez, M. E., Rueda, C. M., Rusie, L. K., Chougnet, C. A. Regulatory T cells control HIV replication in activated T cells through a cAMP-dependent mechanism. Blood. 117, 5372-5380 (2011).
  9. Schulze Zur Wiesch, J., et al. Comprehensive analysis of frequency and phenotype of T regulatory cells in HIV infection: CD39 expression of FoxP3+ T regulatory cells correlates with progressive disease. J. Virol. 85, 1287-1297 (2011).
  10. Kinter, A., et al. Suppression of HIV-specific T cell activity by lymph node CD25+ regulatory T cells from HIV-infected individuals. Proc. Natl. Acad. Sci. U.S.A. 104, 3390-3395 (2007).
  11. Moreno-Fernandez, M. E., Presicce, P., Chougnet, C. A. Homeostasis and function of regulatory T cells in HIV/SIV infection. J. Virol. , (2012).
  12. Angin, M., et al. Preserved Function of Regulatory T Cells in Chronic HIV-1 Infection Despite Decreased Numbers in Blood and Tissue. J. Infect. Dis. 205, 1495-1500 (2012).
  13. Seddiki, N., et al. Expression of interleukin (IL)-2 and IL-7 receptors discriminates between human regulatory and activated T cells. J Exp Med. 203, 1693-1700 (2006).
  14. De Jager, P. L., et al. The role of the CD58 locus in multiple sclerosis. Proc. Natl. Acad. Sci. U.S.A. 106, 5264-5269 (2009).
  15. Baron, U., et al. DNA demethylation in the human FOXP3 locus discriminates regulatory T cells from activated FOXP3(+) conventional T cells. Eur. J. Immunol. 37, 2378-2389 (2007).
  16. Salomon, B., et al. B7/CD28 costimulation is essential for the homeostasis of the CD4+CD25+ immunoregulatory T cells that control autoimmune diabetes. Immunity. 12, 431-440 (2000).
  17. Malek, T. R., Bayer, A. L. Tolerance, not immunity, crucially depends on IL-2. Nat. Rev. Immunol. 4, 665-674 (2004).
  18. Hoffmann, P., Eder, R., Kunz-Schughart, L. A., Andreesen, R., Edinger, M. Large-scale in vitro expansion of polyclonal human CD4(+)CD25high regulatory T cells. Blood. 104, 895-903 (2004).
  19. Putnam, A. L., et al. Expansion of human regulatory T-cells from patients with type 1 diabetes. Diabetes. 58, 652-662 (2009).
  20. Kreijveld, E., Koenen, H. J., Hilbrands, L. B., Joosten, I. Ex vivo expansion of human CD4+ CD25high regulatory T cells from transplant recipients permits functional analysis of small blood samples. J. Immunol. Methods. 314, 103-113 (2006).
  21. Ebinuma, H., et al. Identification and in vitro expansion of functional antigen-specific CD25+ FoxP3+ regulatory T cells in hepatitis C virus infection. J Virol. 82, 5043-5053 (2008).
  22. Strauss, L., Czystowska, M., Szajnik, M., Mandapathil, M., Whiteside, T. L. Differential responses of human regulatory T cells (Treg) and effector T cells to rapamycin. PLoS ONE. 4, e5994 (2009).
  23. Heredia, A., et al. Rapamycin causes down-regulation of CCR5 and accumulation of anti-HIV beta-chemokines: an approach to suppress R5 strains of HIV-1. Proc. Natl. Acad. Sci. U.S.A. 100, 10411-10416 (1073).
  24. Hoffmann, P., et al. Only the CD45RA+ subpopulation of CD4+CD25high T cells gives rise to homogeneous regulatory T-cell lines upon in vitro expansion. Blood. 108, 4260-4267 (2006).
  25. Hoffmann, P., et al. Loss of FOXP3 expression in natural human CD4+CD25+ regulatory T cells upon repetitive in vitro stimulation. Eur. J. Immunol. 39, 1088-1097 (2009).
  26. Wang, J., Ioan-Facsinay, A., vander Voort, E. I., Huizinga, T. W., Toes, R. E. Transient expression of FOXP3 in human activated nonregulatory CD4+ T cells. Eur. J. Immunol. 37, 129-138 (2007).
  27. Takahashi, T., et al. Immunologic self-tolerance maintained by CD25(+)CD4(+) regulatory T cells constitutively expressing cytotoxic T lymphocyte-associated antigen 4. J. Exp. Med. 192, 303-310 (2000).
  28. Thornton, A. M., et al. Expression of Helios, an Ikaros transcription factor family member, differentiates thymic-derived from peripherally induced Foxp3+ T regulatory cells. J. Immunol. 184, 3433-3441 (2010).
  29. Zheng, S. G., Gray, J. D., Ohtsuka, K., Yamagiwa, S., Horwitz, D. A. Generation ex vivo of TGF-beta-producing regulatory T cells from CD4+CD25- precursors. J. Immunol. 169, 4183-4189 (2002).
  30. Gregori, S., Roncarolo, M. G., Bacchetta, R. Methods for in vitro generation of human type 1 regulatory T cells. Methods Mol. Biol. 677, 31-46 (2011).

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