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Soluble CD40 ligand-activated human peripheral B cells as surrogated antigen presenting cells: A preliminary approach for anti-HBV immunotherapy
© Wu et al; licensee BioMed Central Ltd. 2010
Received: 13 October 2010
Accepted: 23 December 2010
Published: 23 December 2010
We aimed to clarify whether soluble CD40 ligand (sCD40L) activated B cells may be loaded with HBcAg18-27 peptide and served as antigen-producing cells (APCs) to induce HBV-specific cytolytic T lymphocytes (CTLs).
Human B cells could be cultured in the presence of sCD40L up to 54 days, and the proportion of B cells in the S phase increased from 0% to 8.34% in the culture. The expression of CD80, CD86, major histocompatibility complex (MHC) classes I and II molecules on the sCD40L-activated B cell was significantly increased after long-time culture. Cytometry and fluorescence microscopy showed that more than 98% sCD40L-activated B cells were loaded by the HBcAg peptide. Furthermore, the peptide-pulsed activated B cells could induce HBcAg18-27 specific CTLs.
Our results demonstrate that sCD40L-activated B cells may function as APCs and induce HBV-specific CTLs.
Efficient antigen presentation by antigen presenting cells (APCs) is critical for inducing T-cell mediated immunity in vivo[1, 2]. Dendritic cells (DCs), activated macrophages, and activated B cells are all capable of presenting antigen peptides. DCs are considered to be highly efficient at antigen capture, processing, and migration . Therefore, DCs have been used to generate antigen-specific T cells for immunotherapy [4–6].
Recently, it has been demonstrated that B cells may function as APCs [1, 7] in addition to the essential role in the humoral immune response. Banchereau et al first reported the "CD40 system" , and suggested to use CD40 ligand (CD40L) stimulated B cells as an alternative or complementary APC. The CD40L-activated B cells may be continually expanded and the B cells significantly up-regulate the expression of major histocompatibility complex (MHC) class I and class II and induce the expression of CD80 and CD86. Antigen-specific CD40L-activated B cells may efficiently endocytose and present antigens, such as protein, RNA, and cDNA, to prime primary T cells and boost robust memory T-cell responses . More importantly, activated B cells may also prime naive T-cell responses against neoantigens ex vivo as DCs do . Thus, the activated B cells may serve as cellular adjuvants to present antigens in vivo.
The mechanism of chronic hepatitis B virus (HBV) infection remains unclear. Previous studies have suggested that functional impairment of DCs may mediate suppression of viral-specific T-cell immune response, resulting in viral persistence in the chronic HBV infection [11–13]. As another type of important APCs, B cells may also function as primary APC in CHB infection . However, little is known whether CD40L-activated B cells may present HBV antigen to T cells.
In this study, we set up an effective culture method for long-term maintenance of B cells in vitro, in which the B cells are activated by human soluble CD40L (sCD40L). Furthermore, we provide evidence that the activated B cells may serve as APCs to present core peptide of HBV to cytolytic T lymphocytes (CTLs).
Proliferation of B cells activated by sCD40L
Additionally, cell cycle profiles analyzed by cell cycle distribution indicated that the G1 phase decreased from 99.87% on day 3 to 88.92% on day 45, concomitant with an increase in cells in the S phase from 0% to 8.34% and the G2/M phase from 0.13% to 2.74% (Figure 1c). However, no decrease in the sub-G1 cells was detected in the culture without sCD40L. The results demonstrated that the B cells were able to re-enter the S phase and proliferate in the presence of sCD40L compared with the cells cultured in the absence of sCD40L. Total number of B cells in the presence of sCD40L increased from 8.84 × 105 to 8.61 × 106, while the number of B cells in the absence of sCD40L was decreased (Figure 1d). Taken together, in accordance with the previous reports , our data demonstrated that B cells may proliferate for significantly long period of time in the presence of sCD40L. After completion of the experiments on the above donor, we repeated all the culture process from another donor's sample; the results were comparable or almost same.
Increased expression of CD80, CD86, MHC classes I and II on cell surface of sCD40L-activated B cells
Visualization of antigen delivery to sCD40L-activated B cells
The result of the HBcAg18-27 specific CTLs
Recently, DC-based immunotherapy has gained a lot of interest in clinical immunology . The high efficiency of DC vaccines has been proved in anti-tumor and anti-virus immunological treatment. However, the DCs constitute only 0.1-0.5% of human PBMC. Technical difficulty and high cost to obtain sufficient number of highly enriched mature DCs have limited the clinical applications of dendritic cell vaccine.
In this study, we used recombinant human GMP-quality trimeric soluble CD40L to activate PBMC-derived B cells. We established and optimized the culture system for CD40L-B cells, which allows B cell activation and proliferation without the contamination from extraneous source germ cells and genes. It was noted that rh sCD40L-activated B cells could be cultured in vitro for up to 54 days under the culture condition. At the same time, B cells significantly up-regulated MHC class I and class II expression and induced expression of CD80 and CD86 after activated by rh sCD40L. Unlike some recent studies, in which B cells were co-cultured with NIH3T3 cells or other tumor cells which steadily express CD40L [8, 19], our results demonstrated that B cells could be activated and expanded for prolonged period of time. While previous culture system has introduced the extraneous source germ cells and has limited the further clinical application researches, the accomplishment of present work may be taken as an alternative way to activate primary human B cells in vitro.
Because sufficient expression of MHC and costimulatory molecules is closely associated with APC function, phenotypic analysis of the cell surface molecules is applied as a reliable surrogate readout for APC function of B cells . Moreover, costimulatory molecules CD80 and CD86 expressed on APCs are required for the development of T cell responses, which play important roles in the differentiation of Th1- or Th2-phenotypes . CD80 and CD86 expressed on the surface of antigen-presenting cells interact with CD28 and cytotoxic T lymphocyte antigen-4 expressed on activated T cells. Interaction between CD80/86 and CD28 mediates critical T cell stimulatory signals, which may cause T cells to stably secrete IL-2 and other cytokines, and maintain T cell survival . Our experiments demonstrate that the rh sCD40L may activate the B cells from PBMCs, and induce a strong up-regulation of those surface molecules associated with antigen processing on human B lymphocytes. Functionally, our study has moved a step forward to demonstrate that 98% of sCD40L-activated B cells may be loaded with HBcAg18-27 peptide. Furthermore, after co-cultured with the peptide-pulsed CD40L-B cells, more HBcAg18-27 specific CTLs were detected in autologous PBMCs. All of these results indicate that the CD40L-B cells have the characteristics of APCs.
The weakness of this study is that all data were just derived from 2 healthy donor samples. However, we performed the experiments separately, not at the same time, i.e., we cultured the B cells from one donor and did the relevant experiments, and then we repeated all the experiments using another donor's sample, the results were comparable or almost same. Thus, we consider that the long-term culture system for B cells developed in this work is reproducible and the data in the present work are sufficient to support our conclusion.
In summary, the present study has established an approach for a long term culture of human B cells from PBMCs under the stimulation of sCD40L and the sCD40L activated B cells may serve as APCs. Furthermore, antigen presenting activity of sCD40L-acitvated B cells was evidenced by antigen-loading and the induction of HBcAg18-27 specific CTLs in autologous PBMCs. Thus, CD40L-activated B cells may be used as a potential source of APCs for adoptive immunotherapy for chronic HBV infection.
Peripheral blood (30 ml) was obtained by venipuncture from two healthy donors with HLA-A2+. The donors gave the consent and all the experiments were approved by the Ethics Committee of Nanjing Drum Tower Hospital, Nanjing University Medical School, in accordance with guidelines of the Nation Health and Medical Research Council of China. PBMCs were isolated by Ficoll-density centrifugation, rinsed twice with iscoves modified Dulbecco medium (IMDM) (Gibco BRL, Carlsbad, USA). Approximately 3 × 107 PBMCs were acquired; 1.6 × 107 PBMCs were further cultured for preparing activated B cells by sCD40L, and the surplus cells were kept in cryopreservation fluid and frozen in liquid nitrogen for pentamer analysis.
Activation of B cells by sCD40L
PBMCs were plated in wells of 6-well plates (8 × 106 cells in 4 ml per well) in IMDM supplemented with 10% human serum with blood type AB, rh IL-4 (2 ng/ml) (R&D Systems, Minneapolis, USA), insulin (5 μg/ml) (Roche, Mannheim, Germany), cyclosporin A (CsA) (5.5 × 10-7 M) (Novartis, Basel, Switzerland), transferrin (50 μg/ml) (Eappel, USA), and gentamicin (15 μg/ml) (Lukang, Shandong, China). Good medical practice (GMP)-quality trimeric rh soluble CD40L (rh sCD40L) (R&D Systems, Minneapolis, USA) was added to a final concentration of 2 μg/ml. The culture was maintained by replacing half medium with the same medium, in which CsA and sCD40L were freshly added. B cells that were cultured in the same medium except that sCD40L were omitted served as controls.
Cell proliferation assay
Cell proliferation was determined by analysis of cell cycle distribution with flow cytometry using Cycle Test Plus DNA Reagent kit (Becton Dickinson, San Jose, USA) as previously described . In brief, the cultured cells (1 × 105) were collected and digested by trypsin, followed by adding trypsin inhibitor and RNAase, then mixed with propidium iodide in the dark condition at 4°C. The cells were then subjected to run on the BD FACSCanto flow cytometer (BD Biosciences, CA, USA). Based on the intensity of the fluorescent light signal emitted by the DNA-binding dye, the cell populations were located in four distinct phases, which may be recognized in static phase (G0/G1), DNA synthesis phase (S), and DNA mitosis phase (M), respectively .
Assay for cell surface molecules
The cell surface molecules, including CD86, CD80, MHC classes I and II, on sCD40L-activated B cells were analyzed by flow cytometry. In brief, 1 × 106 PBMCs in 100 μl PBS were rinsed twice with PBS containing 2% FBS and divided into 3 tubes: anti-CD19-APC, anti-CD86-FITC, and anti-CD80-PE were added into the first tube, anti-CD19-APC, anti-MHC-II-FITC and anti-MHC-I-PE were added into the second tube, and in the third tube, negative isotype control staining reactions were in parallel performed with a saturating concentration of irrelevant mouse IgG1-FITC and IgG1-PE. All above seven antibodies were purchased from BD Biosciences (BD PharMingen, San Diego, CA). After incubated for 20 min and rinsed with PBS, the cells were fixed with 1% paraformaldehyde in PBS. FACS analysis was performed on the BD FACSCanto flow cytometer. B cells were gated on CD19-positive cells for analyzing the cell surface molecules.
Analysis of peptide pulsing
HBV derived peptides were used for peptide pulsing study as previously described [24, 25] with modifications. The HLA-A*0201-binding peptide of HBV core 18-27 (HBcAg 18-27, Phe-Leu-Pro-Ser-Asp-Phe-Phe-Pro-Ser-Val, FLPSDFFPSV), a confirmed HLA-A 2.1-restricted CTL epitope and derived from the HBV core protein , was obtained from Sangon (Shanghai, China). For the MHC class I experiments, the peptide was conjugated by FITC at the first residue of the N-terminus. CD40L-activated B cells were harvested from culture, washed 3 times, and resuspended in serum-free IMDM at 2 × 105 cells/ml and seeded into 24-well plates (1 ml/well). After incubation with the FITC-conjugated peptide for 12-18 hours, the cells were harvested, washed, and resuspended in PBS. Fluorescence analysis was performed immediately on the BD FACSCanto flow cytometer for detecting the ratio of B cells specific binding of HBV core peptide. The residual cells were observed by fluorescence microscope (Zeiss, Goettingen, Germany) for determining the location of HBV core peptide in B cells. B cells were also incubated with no FITC-conjugated peptide under the same condition for pentamer analysis.
On day 45 of B cells culture from one donor, the CD40L-activated B cells were used as the source of APCs for stimulation of autologous T cells. In brief, the frozen PBMCs were rapidly thawed in a 37°C water bath and then cultured at a concentration of 2 × 106 cells/ml in RPMI 1640 supplemented with 10% fetal bovine serum and rhIL-2 (10 ng/ml) (R&D Systems). On day 4, the cultures were replaced with the same medium, followed by co-culture with the peptide-pulsed CD40L-activated B cells. After 4 days, the cells were harvested, washed, and mixed with both anti-CD8-FITC and PE-labeled HLA-A2 pentamer complexes against the HBV core 18-27 peptide (ProImmune, Oxford, UK). The cells were resuspended in 500 μl of PBS and two-colour analysis was performed by BD FACSCanto flow cytometer. For each analysis, 100 000 events were acquired. PBMCs that were cultured in the same medium omitted peptide-pulsed CD40-B served as controls.
This work was supported by grants from National Natural Science Foundation of China (No. 30872234) and grants from Ministry of Public Health of the People's Republic of China, MOPH (No. WKJ2006-2-9).
- Steinman RM: The dendritic cell system and its role in immunogenicity. Annu Rev Immunol 1991, 9: 271-296. 10.1146/annurev.iy.09.040191.001415PubMedView ArticleGoogle Scholar
- Banchereau J, Steinman RM: Dendritic cells and the control of immunity. Nature 1998, 392: 245-252. 10.1038/32588PubMedView ArticleGoogle Scholar
- Cella M, Sallusto F, Lanzavecchia A: Origin, maturation and antigen presenting function of dendritic cells. Curr Opin Immunol 1997, 9: 10-16. 10.1016/S0952-7915(97)80153-7PubMedView ArticleGoogle Scholar
- Chang JW, Hsieh JJ, Shen YC, Ho E, Chuang CK, Chen YR, Liao SK, Chen JS, Leong SP, Hou MM, Chang NJ, Wang CH: Immunotherapy with dendritic cells pulsed by autologous dactinomycin-induced melanoma apoptotic bodies for patients with malignant melanoma. Melanoma Res 2009, 19: 309-315. 10.1097/CMR.0b013e32832b2717PubMedView ArticleGoogle Scholar
- Cao DY, Yang JY, Yue SQ, Tao KS, Song ZS, Wang DS, Yang YL, Dou KF: Comparative analysis of DC fused with allogeneic hepatocellular carcinoma cell line HepG2 and autologous tumor cells as potential cancer vaccines against hepatocellular carcinoma. Cell Immunol 2009, 259: 13-20. 10.1016/j.cellimm.2009.05.007PubMedView ArticleGoogle Scholar
- Chen W, Zhang Z, Shi M, Chen L, Fu J, Shi F, Zhang B, Zhang H, Jin L, Wang FS: Activated plasmacytoid dendritic cells act synergistically with hepatitis B core antigen-pulsed monocyte-derived dendritic cells in the induction of hepatitis B virus-specific CD8 T-cell response. Clin Immunol 2008, 129: 295-303. 10.1016/j.clim.2008.07.026PubMedView ArticleGoogle Scholar
- Coughlin CM, Vance BA, Grupp SA, Vonderheide RH: RNA-transfected CD40-activated B cells induce functional T-cell responses against viral and tumor antigen targets: implications for pediatric immunotherapy. Blood 2004, 103: 2046-2054. 10.1182/blood-2003-07-2379PubMedView ArticleGoogle Scholar
- Schultze JL, Michalak S, Seamon MJ, Dranoff G, Jung K, Daley J, Delgado JC, Gribben JG, Nadler LM: CD40-activated human B cells: an alternative source of highly efficient antigen presenting cells to generate autologous antigen-specific T cells for adoptive immunotherapy. J Clin Invest 1997, 100: 2757-2765. 10.1172/JCI119822PubMedPubMed CentralView ArticleGoogle Scholar
- Coughlin CM, Vonderheide RH: Targeting adult and pediatric cancers via cell-based vaccines and the prospect of activated B lymphocytes as a novel modality. Cancer Biol Ther 2003, 2: 466-470.PubMedView ArticleGoogle Scholar
- Kondo E, Topp MS, Kiem HP, Obata Y, Morishima Y, Kuzushima K, Tanimoto M, Harada M, Takahashi T, Akatsuka Y: Efficient generation of antigen-specific cytotoxic T cells using retrovirally transduced CD40-activated B cells. J Immunol 2002, 169: 2164-2171.PubMedView ArticleGoogle Scholar
- van der Molen RG, Sprengers D, Binda RS, de Jong EC, Niesters HG, Kusters JG, Kwekkeboom J, Janssen HL: Functional impairment of myeloid and plasmacytoid dendritic cells of patients with chronic hepatitis B. Hepatology 2004, 40: 738-746. 10.1002/hep.20366PubMedView ArticleGoogle Scholar
- Beckebaum S, Cicinnati VR, Dworacki G, Müller-Berghaus J, Stolz D, Harnaha J, Whiteside TL, Thomson AW, Lu L, Fung JJ, Bonham CA: Reduction in the circulating pDC1/pDC2 ratio and impaired function of ex vivo -generated DC1 in chronic hepatitis B infection. Clin Immunol 2002, 104: 138-150. 10.1006/clim.2002.5245PubMedView ArticleGoogle Scholar
- Beckebaum S, Cicinnati VR, Zhang X, Ferencik S, Frilling A, Grosse-Wilde H, Broelsch CE, Gerken G: Hepatitis B virus-induced defect of moncyte-derived dendritic cells leads to impaired T helper type l response in vitro : mechanisms for viral immune escape. Immunology 2003, 109: 487-495. 10.1046/j.1365-2567.2003.01699.xPubMedPubMed CentralView ArticleGoogle Scholar
- Milich DR, Chen M, Schödel F, Peterson DL, Jones JE, Hughes JL: Role of B cells in antigen presentation of the hepatitis B core. Proc Natl Acad Sci USA 1997, 94: 14648-14653. 10.1073/pnas.94.26.14648PubMedPubMed CentralView ArticleGoogle Scholar
- Kondo E, Gryschok L, Klein-Gonzalez N, Rademacher S, Weihrauch MR, Liebig T, Shimabukuro-Vornhagen A, Kochanek M, Draube A, von Bergwelt-Baildon MS: CD40-activated B cells can be generated in high number and purity in cancer patients: analysis of immunogenicity and homing potential. Clin Exp Immunol 2009, 155: 249-256. 10.1111/j.1365-2249.2008.03820.xPubMedPubMed CentralView ArticleGoogle Scholar
- Zhu F, Ramadan G, Davies B, Margolis DA, Keever-Taylor CA: Stimulation by means of dendritic cells followed by Epstein-Barr virus-transformed B cells as antigen-presenting cells is more efficient than dendritic cells alone in inducing Aspergillus f16-specific cytotoxic T cell responses. Clin Exp Immunol 2008, 151: 284-296. 10.1111/j.1365-2249.2007.03544.xPubMedPubMed CentralView ArticleGoogle Scholar
- Ivanov R, Aarts T, Hagenbeek A, Hol S, Ebeling S: B-cell expansion in the presence of the novel 293-CD40L-sCD40L cell line allows the generation of large numbers of efficient xenoantigen-free APC. Cytotherapy 2005, 7: 62-73. 10.1080/14653240510018055PubMedView ArticleGoogle Scholar
- Akbar SM, Horiike N, Onji M: Immune therapy including dendritic cell based therapy in chronic hepatitis B virus infection. World J Gastroenterol 2006, 12: 2876-2883.PubMedPubMed CentralGoogle Scholar
- Yoon SH, Cho HI, Kim TG: Activation of B cells using Schneider 2 cells expressing CD40L for the enhancement of antigen presentation in vitro . Exp Mol Med 2005, 37: 567-574.PubMedView ArticleGoogle Scholar
- Noorchashm H, Reed AJ, Rostami SY, Mozaffari R, Zekavat G, Koeberlein B, Caton AJ, Naji A: B cell-mediated antigen presentation is required for the pathogenesis of acute cardiac allograft rejection. J Immunol 2006, 177: 7715-7722.PubMedView ArticleGoogle Scholar
- Chakraborty NG, Li L, Sporn JR, Kurtzman SH, Ergin MT, Mukherji B: Emergence of regulatory CD4+ T cell response to repetitive stimulation with antigen-presenting cells in vitro : implications in designing antigen-presenting cell-based tumor vaccines. J Immunol 1999, 162: 5576-5583.PubMedGoogle Scholar
- Salomon B, Bluestone JA: Complexities of CD28/B7: CTLA-4 costimulatory pathways in autoimmunity and transplantation. Annu Rev Immunol 2001, 19: 225-252. 10.1146/annurev.immunol.19.1.225PubMedView ArticleGoogle Scholar
- Nunez R: DNA measurement and cell cycle analysis by flow cytometry. Curr Issues Mol Biol 2001, 3: 67-70.PubMedGoogle Scholar
- Bocchia M, Korontsvit T, Xu Q, Mackinnon S, Yang SY, Sette A, Scheinberg DA: Specific human cellular immunity to bcr-abl oncogene-derived peptides. Blood 1996, 87: 3587-3592.PubMedGoogle Scholar
- Shi M, Qian S, Chen WW, Zhang H, Zhang B, Tang ZR, Zhang Z, Wang FS: Hepatitis B virus (HBV) antigen-pulsed monocyte-derived dendritic cells from HBV-associated hepatocellular carcinoma patients significantly enhance specific T cell responses in vitro . Clin Exp Immunol 2007, 147: 277-286. 10.1111/j.1365-2249.2006.03281.xPubMedPubMed CentralView ArticleGoogle Scholar
- Penna A, Chisari FV, Bertoletti A, Missale G, Fowler P, Giuberti T, Fiaccadori F, Ferrari C: Cytotoxic T lymphocytes recognize an HLA-A2-restricted epitope within the hepatitis B virus nucleocapsid antigen. J Exp Med 1991, 174: 1565-1570. 10.1084/jem.174.6.1565PubMedView ArticleGoogle Scholar
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