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Blood, 15 September 2004, Vol. 104, No. 6, pp. 1671-1678. Prepublished online as a Blood First Edition Paper on May 27, 2004; DOI 10.1182/blood-2004-03-1115.
HEMATOPOIESIS Bystander destruction of hematopoietic progenitor and stem cells in a mouse model of infusion-induced bone marrow failureFrom the Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD.
Infusion of parental lymph node (LN) cells into sublethally irradiated hybrid F1 recipients created a murine model for bone marrow (BM) failure. Affected animals developed fatal pancytopenia within 2 to 3 weeks, accompanied by BM oligoclonal T-cell infiltration and severe marrow hypoplasia indicated by approximately 10-fold declines in total BM cellularity, 15-fold declines in BM Lin-Sca1+c-Kit+ cells, 100-fold declines in spleen colony-forming units, and 100-fold declines in hematopoietic progenitor and stem cells as estimated by irradiation protection in vivo. LN cells of both H2b/b and H2d/d haplotypes were effectors. Serum interferon-  (IFN-) concentration increased 2- to 3-fold. Marrow cells were severely apoptotic, with high proportions of Fas+ and annexin V+ cells. Cotransplantation of 5 x 105 BM cells from clinically affected donors and 106 BM cells from H2 identical healthy mice could not rescue lethally irradiated recipients. Recipients had significantly lower cellularity in peripheral blood and BM, and cell mixtures failed to produce a stromal feeder layer to support marrow cell growth in vitro. Pathogenic T cells from donors after BM failure appeared capable of destroying hematopoietic progenitor, stem, and stromal cells from fully compatible healthy donors as "innocent bystanders." This effect can be partially abrogated by anti-IFN- antibody. (Blood. 2004;104:1671-1678)
Bone marrow (BM) failure occurs in several closely related human diseases, including aplastic anemia (AA), myelodysplastic syndromes (MDS), and paroxysmal nocturnal hemoglobinuria (PNH). A decrease in the number and function of hematopoietic stem and progenitor cells leads to anemia, neutropenia, and thrombocytopenia, which, when severe and untreated, are fatal.1,2 In all these syndromes, clinical observations and laboratory studies have implicated activated cytotoxic T cells, producing type 1 cytokines, as the effectors of an active process of stem cell destruction, mainly through Fas-mediated apoptosis.2 BM failure can be cured by stem cell replacement from an allogeneic donor, and it can be alleviated by immunosuppressive drugs that allow the recovery of hematopoietic function.2An immune mechanism is dramatically illustrated by transfusion-associated graft-versus-host disease (GVHD), in which foreign donor lymphocytes contained in a blood product and infused into a susceptible host provoke uniformly lethal marrow aplasia.3 Animal models have been developed to better understand the pathophysiology of BM failure and to test new treatments.4-15 In mice, the alkylating drug busulfan produces latent AA. After a course of therapy, animals maintain normal blood counts and bone marrow cellularity for a year before demonstrating pancytopenia and frank aplasia. Spleen colony-forming units (CFU-Ss), representative of early hematopoietic progenitor cells, decline during this intervening period to very low numbers.6 This busulfan-induced model was useful for assessing myelotoxic agents, and it illustrated the enormous compensatory capacity of the marrow, which allows limited numbers of stem cells to provide normal levels of blood cells, but it did not address the likely immune mechanism of most acquired hematopoietic failure in humans. Marrow failure has also been produced in some mouse strains through inoculation of allogeneic lymphocytes.5,7,12 Barnes and Mole4 transplanted 1-10 x 106 C3H/H lymph node (LN) cells into sublethally irradiated CBA/H mice and found that variable numbers of recipients with marrow aplasia eventually died within days or weeks. This approach was extended to C3H/He mice by injecting LN cells from B10.BR mice; donor and recipient shared the same H2k haplotype but differed in a mixed lymphocyte reaction locus (Mls).15 Total body irradiation (TBI) at 6 Gy plus injection of 10 million B10.BR LN cells produced fatal pancytopenia in C3H/He mice within 2 to 3 weeks, accompanied by dramatic declines in CFU-S and colony-forming cells (CFU-Cs) in vitro. However, this model could not be extended to other strains12; mice were H2k identical but Mls mismatched, but certain Mls combinations induced marrow aplasia in one strain combination but not in others. Despite speculation that a macrophage-like cell might be a mediator of immunologic injury,12,13 T lymphocytes, not B cells, were later shown to be responsible for marrow aplasia.7
In the current study, we induced BM failure using the combination of sublethal TBI and parent into hybrid F1 (major histocompatibility complex [MHC]-mismatch) LN cell infusion and specifically studied the effects of infusion-induced BM failure on the phenotype and function of BM hematopoietic progenitor and stem cells. In this model, massive lymphocyte infiltration in the BM led to rapid destruction of hematopoietic progenitor and stem cells. Using a cotransplantation approach, we showed that hematopoietic progenitor and stem cells could be eliminated as "innocent bystanders," not necessarily as specific targets. We also showed that the indiscriminate destruction of BM cells can be partially abrogated by anti-interferon-
Mice and induction of BM failure Inbred C57BL/6 (B6, H2b/b) and BALB/cBy (BALB, H2d/d) mice, hybrid B6D2F1 (H2b/d) and CByB6F1 (H2b/d) mice, and B6-CD45.1 congenic mice were purchased from the Jackson Laboratory (Bar Harbor, ME). They were maintained at animal facilities of the National Institutes of Health and received standard care and nutrition.16 Males and females were used at 6 to 16 weeks of age. Donor and recipient animals were matched for sex in each specific experiment. Inguinal, axillary, and lateral axillary LNs were removed from B6 or BALB donor mice, homogenized in phosphate-buffered saline (PBS) using a mini-tissue grinder (A. Daigger & Company, Vernon Hills, IL), filtered through 100-µm nylon mesh (Small Parts, Miami Lakes, FL), washed in PBS, and counted using a Z2 Coulter Counter (Coulter, Hialeah, FL). In some experiments, each B6D2F1 or CByB6F1 mouse received 5 to 6 Gy TBI from a Gammacell 40 (K2K 1 x 8; MDS Nordion, Ontario, Canada) source at approximately 0.9 Gy/min and was injected with a single dose of 5 to 10 x 106 B6 or BALB LN cells through the lateral tail vein 4 to 6 hours after irradiation. Treated mice received normal care and nutrition and were monitored 2 to 3 times a week until they died or were humanely killed for tissue/cell collection. In 1 experiment, LN cell-infused and untreated mice were killed at day 14 after LN cell infusion and were examined for gross GVHD-related lesions in the skin, liver, stomach, intestines, and spleen. Complete blood cell (CBC) counts were performed on these same mice to ensure that pancytopenia had developed. Cellular composition analyses Mice received no treatment (untreated) or they received 5 to 6 Gy TBI (TBI only), 5 to 6 Gy TBI plus 5 to 10 x 106 B6 LN cells (B6 LN cells), or 5 Gy TBI plus 10 x 106 BALB LN cells (BA-LN cells) and were bled from the retro-orbital sinus 14 to 21 days after LN cell injection. Red blood cells (RBCs) and white blood cells (WBCs) were analyzed using a Z2 Coulter Counter in experiments 1 and 3, whereas CBCs were performed in experiment 4 using a Hemavet 1500 analyzer (Drew Scientific, Oxford, CT). Some experimental mice were humanely killed at 14 to 21 days after treatment, and BM cells were extracted from tibiae and femurs of both legs, counted with a Coulter Counter, and processed for further analysis or transplantation.
Procedures for flow cytometry were as previously described.17 To lyse RBCs, peripheral blood and BM cells were incubated twice in Gey solution (130.68 mM NH4Cl, 4.96 mM KCl, 0.82 mM Na2HPO4, 0.16 mM KH2PO4, 5.55 mM dextrose, 1.03 mM MgCl2, 0.28 mM MgSO4, 1.53 mM CaCl2, and 13.39 mM NaHCO3) for 10 minutes each incubation. After that, they were stained and washed in flow buffer (2.68 mM KCl, 1.62 mM Na2HPO4, 1.47 mM KH2PO4, 137 mM NaCl, 7.69 mM NaN3, and 1% bovine serum albumin [BSA]), first with a premixed antibody cocktail and then with diluted streptavidin-conjugated quantum red (SAQR). Monoclonal antibodies directed against murine CD3 (clone 145-2C11), CD4 (clone GK 1.5), CD8 (clone 53-6.72), CD11b (clone M1/70), CD19 (clone ID3), CD34 (clone RAM34), CD45R (B220; clone RA3-6B2), CD95 (Fas; clone Jo2), CD117 (c-Kit; clone 2B8), erythroid cells (clone Ter119), granulocytes (Gr1/Ly6-G; clone RB6-8C5), stem cell antigen 1 (Sca1; clone E13-161), and a panel of 15 T-cell receptor- ELISA
Orbital sinus blood was kept at room temperature (RT) for 30 minutes and then underwent centrifugation at 1020g for 10 minutes. Serum was removed and stored at -20°C. Serum IFN- CFU-S and irradiation protection assays Ten CByB6F1 mice each received 5 Gy TBI, and 5 x 106 LN cells from B6-CD45.1 donors were killed on day 14. BM cells were extracted from 2 tibiae and 2 femurs of each mouse and were combined to form 3 pools (P1, mice 1-4; P2, mice 5-7; P3, mice 8-10). Cells from P2 and P3 were injected into 4 lethally irradiated (10 Gy; Gammacell 40; MDS Nordion, Ontario, Canada) CByB6F1 recipients at 105 cells per recipient. Eight more recipients each receiving 105 BM cells from 2 healthy CByB6F1 donors were used as controls. After 12 days, all 16 recipients were killed, and spleens were removed for examination of colonies. Numbers of colonies per 105 BM cells were multiplied by total numbers of BM cells per mouse to calculate total CFU-S per mouse. BM cells in P1 (from treated mice 1-4) were washed once in PBS and were resuspended in 4 mL PBS. Half these cells were injected into 4 lethally irradiated (10 Gy) CByB6F1 recipients at 0.5 mL cells per recipient, equivalent to 50% BM cells from the 2 tibiae and 2 femurs of each donor mouse (1:2 dilution), and the remaining cells (2 mL) were transferred to a new tube and were combined with 2 mL PBS. This process was carried out for 6 dilutions from 1:2 to 1:64. We injected cells from each dilution into 4 lethally irradiated recipients. In parallel, BM cells from 2 untreated CByB6F1 control donors were diluted from 1:32 to 1:128 and were injected into lethally irradiated CByB6F1 recipients. Recipient survival was monitored for 2 months. Cotransplantation B6D2F1 or CByB6F1 mice treated with 5 Gy TBI (TBI only) plus 5 x 106 B6 LN cells (B6 LN cells) were humanely killed 14 to 15 days after initial treatment. BM cells extracted from each donor mouse were mixed 1:2 with BM cells from a B6-CD45.1 congenic standard mouse, and the cell mixtures were injected into new sets of lethally irradiated (11 Gy; Gammacell 40; MDS Nordion), young B6D2F1 or CByB6F1 recipients. Each recipient was injected with 5 x 105 BM cells from a designated donor and 106 BM cells from the B6-CD45.1 congenic standard. Recipient survival was monitored 2 to 3 times per week for the first 4 weeks. In both experiments, recipients alive at 10 weeks after transplantation were bled and analyzed for donor contribution by flow cytometry.
In other experiments, CByB6F1 recipients were divided into 4 treatment groups: (1) BM failure plus B6-CD45.1 donor cells with 500 µg anti-IFN- Stromal feeder layer development and cell culture
BM cells from CByB6F1 mice treated with 5 Gy TBI and 5 x 106 B6 LN cells 14 days earlier were mixed 1:2 with BM cells from a fresh B6 donor, and the cell mixtures were transplanted into a new set of lethally irradiated CByB6F1 recipients at 1.5 x 106 cells per recipient. Two weeks later, BM cells were extracted from 3 recipients and from 2 CByB6F1 mice to establish stromal feeder layers in 96-well, flat-bottomed cell culture plates by culturing in Data analysis Data from blood, BM cell composition analyses, and flow cytometry analyses were analyzed using JMP statistical discovery software (SAS Institute, Cary, NC).18 Data were presented as mean ± SEM, and statistical significance was declared at the P less than .05 and P less than .01 levels.
Induction of BM failure We induced BM failure by infusing preirradiated hybrid B6D2F1 and CByB6F1 mice with parental B6 or BALB LN cells. In experiment 1, 6 Gy TBI plus 10 x 106 B6 LN cell injection caused recipients to die at approximately 12 days, whereas mice that received 6 Gy TBI without LN cell infusion survived without marrow replacement (Table 1). Injecting 10 x 106 B6 LN cells into B6D2F1 mice preirradiated at 5 Gy TBI produced BM failure, as follows: 9-fold reductions in WBC counts (P < .0001), 2.5-fold reductions in RBC counts (P < .0001), and more than 10-fold reductions in total BM cell counts (P < .0001) (Table 2). This success led us to test BM failure induction in a different hybrid strain, CByB6F1. In experiment 2, injecting 5 x 106 or 10 x 106 B6 LN cells into CByB6F1 recipients preirradiated at 5 Gy TBI caused all recipients to die by day 14 (Table 1). In experiment 3, we administered 5 Gy TBI and injected 5 x 106 B6 LN cells into 15 CByB6F1 mice. Seven mice died between days 14 and 21 (Table 1), and the remaining 8 mice showed more than 12-fold reductions in WBC counts (P < .0001) and 3-fold reductions in RBC counts (P < .0001) (Table 2). Thus, sublethal irradiation plus B6 LN cell infusion caused BM failure in B6D2F1 and CByB6F1 hybrid mice.
Because B6 LN cells were effective at inducing BM failure in preirradiated F1 mice, we next questioned whether the marrow-destructive effect was restricted to lymphocytes carrying the H2b/b allele. Toward this end, we conducted experiment 4 in which newly preirradiated CByB6F1 mice were infused with 5 x 106 LN cells from B6 (H2b/b) donors or with 10 x 106 LN cells from BALB (H2d/d) donors. By day 14, 8 of 10 B6 LN cell-injected recipients died (Table 1), and the 2 remaining recipients had severe pancytopenia (Table 2). The 5 recipients that received BALB LN cells were alive but had severe lymphocytopenia, thrombocytopenia, and mild anemia, with 15-fold reductions in WBC counts (P < .0001), 31% reductions in RBC counts (P < .05), 7-fold reductions in platelet counts (P < .0001), and 10-fold reductions in total BM cells (P < .0001) (Table 2). Thus, LN cells from BALB donors of the H2d/d haplotype also induced BM failure in CByB6F1 mice, though LN cells from B6 donors of the H2b/b haplotype appeared more effective. Infusing parental LN cells resulted in BM failure in the hybrid F1 recipients. No gross GVHD-related lesions were found in skin, stomach, intestines, liver, or spleen of 4 mice that were killed on day 14 after LN infusion and had pancytopenia and marrow hypoplasia at the time of analysis. Mice receiving sublethal TBI without injection of parental LN cells had slight decreases in RBC counts, 60% decreases in WBC counts, and 40% decreases in platelet and total BM cell counts compared with untreated control mice, as measured 2 to 3 weeks after irradiation. The degree of pancytopenia in these control animals was more modest than in the experimental group; in addition, all animals showed spontaneous recovery, and no deaths were associated with sublethal TBI (Table 2). Marrow aplasia and lymphocyte infiltration
In addition to peripheral pancytopenia, affected mice also showed severe marrow aplasia with more than 10-fold declines in marrow cellularity on average (Table 2). Affected animals had 2- to 3-fold increases in serum IFN-
To analyze the composition of infiltrated T lymphocytes in the marrow of BM failure mice, we examined selected V
Elimination of functional hematopoietic progenitor and stem cells A characteristic feature of human BM failure syndrome is a deficiency of hematopoietic progenitor and stem cells. We studied the stem cell compartment using 3 different systems. First, we analyzed BM cells for the Lin-Sca1+c-Kit+ marker phenotype and further divided cells into CD34+ and CD34- fractions. It was shown previously that mouse BM Lin-Sca1+c-Kit+CD34- cells contain long-term hematopoietic stem cells, whereas BM Lin-Sca1+c-Kit+CD34+ cells were less primitive.19,20 Compared with control mice, BM failure mice had normal proportions of Lin- cells, drastically reduced (P < .01) proportions of Lin-Sca1+c-Kit+ cells (Figure 3, top panels), and significantly reduced (P < .01) proportions of Lin-Sca1+c-Kit+CD34- and Lin-Sca1+c-Kit+CD34+ cells (Figure 3, bottom panels). Calculated total Lin-Sca1+c-Kit+, Lin-Sca1+c-Kit+CD34+, and Lin-Sca1+c-Kit+CD34- cells per mouse were reduced 17.5-fold, 21-fold, and 14-fold, respectively, in BM failure mice (all at P < .01) (Figure 4, upper left).
Second, we tested hematopoietic progenitor cell function using the day-12 CFU-S assay. The concentration of day 12 CFU-S was reduced 8-fold (P < .01) in BM failure mice (data not shown), equivalent to an overall 82-fold decline (P < .01) in total day-12 CFU-S in BM failure mice compared with untreated controls (Figure 4, upper right), considering the 10- to 11-fold reduction in total BM cells per mouse. Third, we tested the ability of donor BM cells to rescue lethally irradiated recipients. When serially diluted BM cells from BM failure donors and untreated healthy donors were injected into lethally irradiated young animals, cells from BM failure donors could not rescue recipients even at the lowest dilution (1:2); all recipients died within 3 weeks. Cells from healthy control donors prevented recipient death for 2 months at the highest (1:128) dilution tested (Figure 4, bottom). From these data, we estimated a 64- to 128-fold decrease in functional hematopoietic progenitor and stem cells in BM failure mice. Hematopoietic stem cells are destroyed as innocent bystanders Although marrow cell destruction was severe and extensive in LN cell-infused mice, a key question was whether hematopoietic progenitor and stem cells were specifically targeted or were destroyed as innocent bystanders. To address this issue, we examined cell function in vivo in cotransplantation experiments in which BM cells from BM failure B6D2F1 or CByB6F1 donors (previously treated with sublethal TBI and B6 LN cell injection) and control B6D2F1 and CByB6F1 donors (sublethal TBI only) were mixed with BM cells from healthy B6-CD45.1 congenic codonors, and the cell mixtures were then injected into lethally irradiated B6D2F1 recipients. In the first experiment, 3 recipients that received 10 x 105 BM cells from the B6-CD45.1 congenic codonor survived long-term and showed 100% contribution of the transplanted B6-CD45.1 cell type, indicating that 10 x 105 B6-CD45.1 BM cells were sufficient to rescue recipients from lethal irradiation. Five recipients that received 5 x 105 BM cells from a control donor and 10 x 105 cells from the B6-CD45.1 congenic codonor all survived long term and showed engraftment from both the donor and the B6-CD45.1 codonor, whereas 10 recipients that received 5 x 105 BM cells from 1 of the 2 BM failure donors and 10 x 105 BM cells from the B6-CD45.1 congenic codonor all died within 2 to 4 weeks of marrow transplantation (Figure 5A). In a second experiment, the same design was used to test bystander effects in CByB6F1 recipient mice; similar results were obtained: death of recipients of BM failure donor plus codonor cells and normal engraftment in recipients of BM cells from control donor and codonor (data not shown). Thus, marrow cells from BM failure donors not only failed to contribute to recipient reconstitution but also indiscriminately destroyed BM cells from the B6-CD45.1 congenic codonors as bystanders, preventing engraftment and causing recipient death.
Because recipients of BM cell mixtures from BM failure donors and congenic codonors had all died within 2 to 4 weeks in both experiments, we conducted another experiment in which some of the recipients were analyzed at an earlier time point. We also tested the potential role of anti-IFN- Destruction of BM stromal cells as bystanders To investigate whether bystander cell destruction damaged not only hematopoietic cells but also stromal cells, we cotransplanted BM cells from BM failure CByB6F1 mice with BM cells from a healthy B6 codonor into lethally irradiated CByB6F1 recipients. Two weeks later, BM cells from humanely killed recipients were cultured in 96-well plates to develop feeder layers; at 4 weeks, they were overlaid with fresh BM cells from an untreated healthy CByB6F1 donor. For comparison, feeder layers were also established from BM cells of untreated healthy CByB6F1 mice, which were then overlaid with fresh BM cells from the same untreated healthy CByB6F1 donor. Stromal feeder layers that developed from normal CByB6F1 BM cells supported marrow cell growth (Figure 6, upper panel), but BM cells from cotransplantation recipients did not form a stromal feeder layer and thus could not support the growth of overlaid normal BM cells (Figure 6, low panel). These data indicate that BM cells from BM failure donors indiscriminately destroyed stromal cells from BM of healthy codonors, causing functional failure in the establishment of a feeder layer to support marrow cell growth (Figure 6, low panel).
In our mouse model, injecting 5-10 x 106 LN cells of a parent animal into sublethally irradiated F1 recipients produced a disease that closely resembled human BM failure. RBC, WBC, and platelet counts dramatically decreased within 2 to 3 weeks to levels approximately 10% to 20% of normal, and severe pancytopenia was accompanied by profound marrow aplasia. These are clinical characteristics of human AA.2 Infused donor LN cells infiltrated and expanded in recipient BM; these cells are likely the effectors of the massive destruction of more than 90% of all cells in the BM. Lack of typical GVHD responses in tissues other than BM, such as skin, stomach, intestines, liver, and spleen, is a useful if not fully explained feature of this mouse model. In a previous study, Ellison et al21 reported that infusing 100 x 106 B6 LN-spleen cell mixture into healthy B6D2F1 mice induced acute GVHD responses, with apoptotic lesions in recipient intestines 2 weeks after cell infusion. BM was not examined. It may be that we did not observe gross intestinal damage because of our lower dose of LN cells in the infusion and because BM is more vulnerable than intestine in acute GVHD. The destruction of functional hematopoietic progenitor and stem cells in our BM failure mouse model was severe and extensive, as evidenced by an approximate 100-fold decline in CFU-S and in cells capable of protecting and repopulating a lethally irradiated recipient (Figure 4). These numbers differ from the approximate 10-fold lower numbers of total BM cells (Table 2) and Lin-Sca1+c-Kit+CD34- cells (Figures 3, 4). The dissociation between the Lin-Sca1+c-Kit+CD34- marker phenotype (Figure 3) and functional hematopoietic stem cells (Figure 4) in BM failure mice is similar to that reported previously for in vivo expanded BM cells22 and for BM cells from Il2-deficient mice.23 The total number of BM cells and Lin-Sca1+c-Kit+CD34- cells likely underestimates the severity of marrow destruction because most residual cells in the BM infiltrated expanded populations of donor T cells (Figure 1), and only a small fraction represent residual host marrow cells.
Activated T lymphocytes, producing type 1 cytokines, cause extensive stem cell destruction and the development of pancytopenia and marrow aplasia in patients with BM failure.24 We compared a 2- to 3-fold increase in serum IFN-
Our results in general are concordant with findings of others in mouse models of autoimmunity in which indiscriminate cell destruction has been assigned 2 distinct mechanisms: cytokine effect and epitope spreading. For viral-induced pancytopenia, perforin-deficient mice infected with lymphocytic choriomeningitis virus (LCMV) showed progressive pancytopenia within 14 days of infection.5 Disease was prevented by depleting CD8+ T lymphocytes and was accelerated by increasing the frequency of LCMV-specific CD8+ T cells. There was no cognate interaction between the TCR and hematopoietic progenitors presenting either the LCMV-derived antigens or self-antigens on the major histocompatibility complex, and damage to hematopoiesis was interpreted as the result of excessive secretion and activity of TNF- We report here that infusing parent LN cells into hybrid F1 recipients induced BM failure in mice that can serve as a model for human immune-mediated BM failure. LN from B6 and BALB donors can provide effector cells. We demonstrate that residual marrow cells from infusion-induced BM failure mice are infiltrated with expanded donor T lymphocytes, which, on mixing with fresh BM cells from healthy donors, were able to destroy H2 identical hematopoietic progenitor and stem cells from healthy BM as innocent bystanders.
We thank Keyvan Keyvanfar from the Hematology Branch and David Caden from the Laboratory of Animal Medicine of the National Heart, Lung, and Blood Institute for technical assistance in flow cytometry and complete blood counts.
Submitted March 24, 2004; accepted May 10, 2004.
Prepublished online as Blood First Edition Paper, May 27, 2004; DOI 10.1182/blood-2004-03-1115.
The publication costs of this article were defrayed in part by page charge payment. Therefore, and solely to indicate this fact, this article is hereby marked "advertisement" in accordance with 18 U.S.C. section 1734.
Reprints: Jichun Chen, Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bldg 10, Rm 7C118, 9000 Rockville Pike, Bethesda, MD 20892-1652; e-mail: chenji{at}nhlbi.nih.gov.
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Abstract
Introduction
variable region (TCR-V
-modified Eagle medium (
