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Blood, 15 November 2008, Vol. 112, No. 10, pp. 4090-4097. Prepublished online as a Blood First Edition Paper on August 26, 2008; DOI 10.1182/blood-2008-04-153361.
IMMUNOBIOLOGY Clinical and immunologic consequences of a somatic reversion in a patient with X-linked severe combined immunodeficiency1 Center for Paediatrics and Adolescent Medicine, University of Freiburg, Freiburg, Germany; 2 Institute for Transfusion Medicine, University Hospital Ulm and Institute for Clinical Transfusion Medicine and Immunogenetics, Ulm, Germany; 3 Institute for Pathology, University of Freiburg, Freiburg, Germany; 4 Department of Paediatrics and Adolescent Medicine, University Hospital, Ulm, Germany; 5 Helios Kliniken Krefeld, Krefeld, Germany; 6 Molecular Immunology Unit, Institute of Child Health, University College London, London, United Kingdom; 7 Institute for Human Genetics, University Hospital Essen, Essen, Germany; 8 Medical Center, Department of Rheumatology and Immunology, University of Freiburg, Freiburg, Germany; and 9 Department of Haematology and Oncology, Olgaspital, Stuttgart, Germany
X-linked severe combined immunodeficiency is a life-threatening disorder caused by mutations in the gene encoding the interleukin-2 receptor gamma chain (IL2RG). Hypomorphic mutations and reversion of mutations in subpopulations of cells can result in variant clinical phenotypes, making diagnosis and treatment difficult. We describe a 5-year-old boy with mild susceptibility to infection who was investigated for a mutation in IL2RG due to persistent natural killer (NK)– and T-cell lymphopenia. A functionally relevant novel T466C point mutation was found in B, NK, and epithelial cells, whereas  /β and  / T cells showed the normal gene sequence, suggesting reversion of the mutation in a common T-cell precursor. This genetic correction in T cells resulted in a diverse T-cell repertoire and significant immunity despite failure to produce specific antibodies linked to an intrinsic defect of mutant B cells. These observations confirm the potential of revertant T-cell precursors to reconstitute immune function, but questions remain on the longevity of revertant cells implicating the need for careful follow up and early consideration of hematopoietic stem cell transplantation (HSCT).
Severe combined immunodeficiency (SCID) is a life-threatening disorder due to impairment of T-cell development, function, or both.1,2 The molecular basis of the clinical syndrome is heterogeneous and includes mutations in genes involved in metabolism, signaling, and DNA repair. The most frequent form of SCID is caused by mutations in the gene encoding the common gamma chain of the interleukin-2 (IL-2) receptor (IL2RG).3 In the absence of a functional c gene, early lymphoid progenitor cells are unable to respond to the cytokine signals of IL-2, IL-4, IL-7, IL-9, IL-15, and IL-21 that are crucial for the normal development of T cells, natural killer (NK) cells, and late-stage B cells.4 Clinically, this X-linked form of SCID is characterized by severe and persistent infections starting in the first months of life typically accompanied by diarrhea and failure to thrive.5 Affected infants lack T cells and NK cells and show hypogammaglobulinemia despite normal B-cell counts. Without bone marrow transplantation, the disease is usually fatal within the first year of life Not all patients with mutations in the IL2RG gene or other genes associated with SCID, however, show the typical phenotype of severe immunodeficiency, rendering the diagnosis more difficult.6–13 In those patients, variable numbers of residual functional T cells attenuate the phenotype. The most common molecular cause for this phenomenon is hypomorphic mutations allowing sufficient function of the affected protein to generate some T cells. T cells can also be acquired by materno-fetal transfusion.14,15 Usually, however, these maternal T cells are poorly functional and not able to significantly attenuate the clinical phenotype.15 One patient with moderate immunodeficiency has been described who carried a point mutation in the IL2RG gene in all investigated epithelial and hematopoietic cells except for T cells.10 This patient most likely had a genetic reversion in a T-cell precursor. This reversion allowed the generation of a surprisingly large repertoire of T cells, leading to a significant attenuation of the clinical phenotype.16 In this study, we describe the clinical and molecular details of a second patient with a genetic reversion of a point mutation in the IL2RG gene in a common T-cell precursor. In addition, we provide clinical follow-up information on the first patient. The results illustrate that a genetic reversion presumably occurring in a single T-cell precursor is sufficient to provide a T-cell repertoire that can turn an otherwise lethal disease into a mild immunodeficiency. However, close monitoring is required because of uncertainty regarding the stability of the clinical and cellular immunologic phenotype.
Informed consent for the performed studies was obtained from the patient's family in accordance with the Declaration of Helsinki and Institutional Review Board approval from the University of Freiburg Ethics Committee. Immunophenotyping Lymphocyte phenotyping was performed with 4-color flow cytometry on a FACScan (BD Biosciences, Cowley, United Kingdom) using antibodies from BD PharMingen (San Diego, CA) and Immunotech (Hamburg, Germany) as described.17,18 TCR CDR3 spectratyping
TCR CDR3 spectratyping was performed as described by Pannetier et al for the analysis of the TCR β chain19,20 and for the TCR Functional T- and B-cell assays Global T-cell proliferation in response to mitogens and antigens was quantified using a standard [3H]thymidine incorporation assay. Proliferation of single CD4+ and CD8+ T cells was determined in a CFSE (5- (and 6-)carboxyfluorescein diacetate succinimidyl ester) proliferation assay.17 For this, CD3+ T cells from the patient and a healthy control were sorted using a "no touch" magnetic beads procedure according to manufacturer's instructions (MACS Cell Separation with Pan T Cell Isolation Kit II; Miltenyi Biotec, Bergisch Gladbach, Germany). To provide "accessory cells," which are needed for an appropriate response to phytohemagglutinin (PHA), the T cells were supplemented with autologous CD3-depleted PBMCs at a ratio of 1:1. The cell mixture was labeled with CFSE and plated at 2 x 105 cells per well for stimulation with 1.25 µg/mL PHA or with 10 µL anti-CD3/anti-CD28–coated beads (Dynabeads CD3/CD28 T Cell Expander; Dynal Biotech, Hamburg, Germany). After 6 days of culture, the cells were stained with anti-CD4 and anti-CD8 antibodies and the CFSE dilution was determined by flow cytometry. Cytotoxic T lymphocyte (CTL) degranulation and interferon-gamma production were studied in day-2 PHA blasts using antibodies against CD107a and CD107b as described previously.21 B-cell function in vitro was tested as described previously.18 STAT5 and STAT6 tyrosine phosphorylation assays IL-2 (104 units; Chiron, Berkshire, United Kingdom) or IL-4 (5 ng/mL; R&D Systems, Abington, United Kingdom) was added to 106 PBMCs or Epstein-Barr virus (EBV)–transformed lymphoblastoid cell lines (LCLs), incubated at 37°C for 10 minutes, followed by addition of FACS Lyse/Fix (BD Biosciences) according to the manufacturer's instructions. After washing the cells with phosphate-buffered saline (PBS)/1% fetal calf serum (FCS), cold Perm Buffer III (BD Biosciences) was added followed by antibodies (STAT5 ptyr Alexa 468, STAT6 ptyr phycoerythrin [PE], and CD4 peridinin chlorophyll protein [PerCP], BD Biosciences) according to the manufacturer's instructions. The cells were then washed and fixed (FACSFix; BD Biosciences). Ten thousand lymphocyte events were acquired (FACSCalibur; BD Biosciences) and analyzed using CellQuest software (BD Biosciences). Genetic analysis Genomic DNA covering the IL2RG gene was amplified with primer pairs for all exons, including intron-exon boundaries yielding overlapping amplimers. These amplimers were sequenced in both directions. Primer sequences for amplification and sequencing are available on request (klaus.schwarz{at}uni-ulm.de). Lymphocyte subsets were sorted using a MoFlo high-speed cell sorter (Dako, Carpinteria, CA) to more than 90% purity before DNA extraction for genetic analysis. Short tandem repeat (STR) analysis was performed with the AmpF/STR Identifier PCR amplification kit (Applied Biosystems) according to the manufacturer's description. Three-dimensional modeling of the IL2R common gamma chain was based on the IL2RG structural data deposited in the RCSB-PDB database22 using the Swiss-PdbViewer,23 which is available at http://www.expasy.org/spdbv (The Swiss Institute of Bioinformatics). X-inactivation analysis To assess the inactivation status of the X chromosome, the methylation status of the fragile X mental retardation gene locus (FMR1)24 was studied, because the androgen receptor locus was not informative in this family. Undigested DNA samples and DNA samples digested with the methylation-sensitive enzyme HpaII were amplified with fluorescence-tagged PCR primers flanking the CGG repeat within the FMR1 gene.24 A PCR fragment derived from a plasmid vector containing 4 HpaII sites as well as DNA from a male donor was included as a control for complete HpaII digestion. PCR products were analyzed on an ABI 3100 capillary genetic analyzer and GeneScan and Genotyper software (Applied Biosystems). The degree of X inactivation was calculated as (pd1/pu1)/(pd1/pd1 + pd2/pd2), where pd1 and pd2 represent the peak integrals of the stronger and weaker HpaII-digested allele, respectively, and pu1 and pu2 are the corresponding peak integrals from the undigested samples. Primer sequences are as follows: FMR1F, 5'-GCTCAGCTCCGTTTCGGTTTCACTTCCGGT-3' and FMR1r, 5'-AGCCCCGCACTTCCACCACCAGCTCCTCCA-3'.
Case report The patient (P2) is the first child of nonconsanguineous healthy German parents. A maternal uncle died at the age of 6 months following recurrent pneumonias. Apart from several episodes of mild obstructive bronchitis, the medical history was unremarkable until the age of 14 months, when he presented with diffuse eruptions of round erythematous papular skin lesions. A biopsy showed granulomas but no evidence for fungal or mycobacterial infection. The lesions spontaneously resolved with some scarification over a period of 8 months. At the age of 21 months he was admitted for septic infection with Salmonella enteritidis that responded well to antibiotic therapy. In the following 4 months, 3 episodes of fever and neutropenia were noted. All of these episodes responded well to antibiotics; microorganisms could not be isolated. Neutropenia was thought to be infection associated and eventually resolved, but lymphopenia of around 10 x109/L (1000/µL) persisted, leading to further immunologic investigations described in "Basic immunologic findings." The molecular diagnosis was established at 5 years of age. Until then, the boy had been without specific treatment. Measles, mumps, and rubella (MMR) live vaccine was tolerated without complications. He was started on prophylactic cotrimoxazol and on subcutaneous immunoglobulin substitution after the finding of mild bronchiectasis. Under this therapy, the patient is presently 6.5 years old and in excellent health with no more significant episodes of bronchitis. Basic immunologic findings
Between the age of 5 and 7 years, immunologic investigations of P2 (Table 1) showed a low number of circulating T cells (470-1050/µL) with a CD4/CD8 ratio below 1 and a significantly increased percentage of
Genetic analysis
Because of the cellular phenotype (Tlow, NKlow) and the family history, the gene encoding
Functional relevance of the c mutationSince the mutation has not been described previously, we sought to assess its functional relevance. Normal levels of CD132 were detected on the patient's B cells, indicating that the mutation did not affect protein expression (Figure 2A). CD132-dependent signal transduction was analyzed by determining STAT-5 phosphorylation after IL-2 stimulation and STAT-6 phosphorylation after IL-4 stimulation of EBV-transformed B-cell lines. The use of these cell lines allowed including a control from a patient with a known loss-of-function mutation (c.545G>A [Cys182Tyr]) in the IL2RG gene. We did not detect STAT-5 phosphorylation in response to IL-2 (Figure 2B), but did detect residual STAT-6 phosphorylation in response to IL-4 (Figure 2C). This result was confirmed in fresh B cells (Figure 2D), indicating that the Leu151Pro mutation in CD132 allowed some signaling, at least when paired with the IL-4 receptor alpha chain. The absence of mutated T cells in the patient suggested, however, that the mutation did not allow significant T-cell development. To provide further evidence for this, we analyzed the X-inactivation pattern in the maternal T cells. Whereas unsorted PBMCs showed no preferential X-inactivation pattern, sorted T cells exclusively expressed a single allele, demonstrating the selective advantage for cells expressing this allele (Figure 2E). Although no further data were available from the maternal uncle, the severe course of his illness is also compatible with an important functional impact of this mutation on signals required for T-cell development.
T-cell repertoire developing from the revertant precursor
We then analyzed the diversity of the T-cell repertoire generated by the revertant T-cell precursor. Analysis of Vβ usage among CD4+ and CD8+ T cells using 21 Vβ–specific antibodies revealed a mildly skewed repertoire that was more perturbed among CD8+ than among CD4+ T cells, compared with age-matched controls25 (Figure 3A). For higher resolution of the repertoire analysis, we performed TCR CDR3 spectratyping. Overall, the patient showed a surprisingly wide CDR3 size distribution, which was similar to a representative 6-month-old control in many of the Vβ families (Figure 3B). Among the Vβ 1, 7, 8, 13, or 22 families, both the number of distinct CDR3 lengths as well as the size distribution of the present peaks deviated from the control. However, lack of a sufficient number of appropriate age-matched control samples did not allow statistical evaluation of this difference. Since the patient had an unusually high percentage of T cells expressing the
Functional analysis of T and B cells
Given the normal ILRG sequence in the patient's T cells, the reduced proliferative response of T cells was unexpected. To further determine the functional status of the revertant T cells, we analyzed STAT-5 phosphorylation in response to IL-2, which was found to be normal (Figure 4A). We then performed CFSE proliferation assays, which allowed the detection of the proliferative response in single cells rather than the overall response of a bulk culture. To correct for the lower fraction of T cells among PBMCs in the patient sample, we isolated CD3+ T cells and supplemented them with autologous CD3-depleted PBMCs at a ratio of 1:1 to provide the "accessory cells" required for an appropriate response to mitogens. The response of CD8+ as well as of CD4+ T cells from the patient was similar to a healthy control both after PHA and after anti-CD3/anti-CD28 stimulation (Figure 4B). These data suggest that the impaired responses in the thymidine incorporation assay (Table 1) were due to the low number of T cells and not due to a principal defect in T-cell proliferation. We also analyzed the ability of PHA blasts to produce IFN-
Although residual STAT-6 phosphorylation was detectable in the patient's B cells, he failed to produce specific antibodies to most antigens. We therefore determined the differentiation status of his B cells and found a normal fraction of mature IgM+IgD+CD21+ B cells with few transitional B cells, but few CD27+ non–class-switched and class-switched memory B cells, suggesting impaired terminal B-cell differentiation. (Figure 5A). We then analyzed the ability of the patients PBMCs to respond to stimulation with the mitogens PWM (a T cell–dependent stimulus) and SAC plus IL-2 (T-cell independent for memory B cells). Both stimuli did not induce significant IgM or IgG production, although some IgA production was observed. These data suggest that the lack of specific antibodies was due to an intrinsic defect in the mutated B cells.
In this study, we describe the clinical and immunologic consequences of a somatic reversion in a common T-cell precursor for a child with a novel T466C mutation in the IL2RG gene. The mutation impaired tyrosine phosphorylation of STAT-5 in response to IL-2 and led to severely impaired development of T cells as indicated by the absence of mutated T cells in the child and the completely skewed X inactivation in the T cells of the mother.26 The mutation also severely impaired NK-cell development.27 The few detected NK cells carried the mutation and may reflect either residual NK-cell development in the absence of c28 or some remaining IL-15 signaling.
The The coexistence of revertant T cells and mutant B cells in our patient represents a naturally occurring experiment, allowing for the long-standing question of whether B cells are intrinsically defective in X-SCID to be addressed. It has been shown previously that IL-4–dependent functional responses such as proliferation, IgE secretion, and CD23 expression can occur in mutant B cells.37 However, another study showed that the residual IL-4 signaling in the absence of IL2RG is not sufficient for completely normal B-cell function.30 In line with these findings, in B cells from P2, STAT-6 phosphorylation in response to IL-4 was detectable, but significantly reduced, and there was no immunoglobulin production in vitro in response to mitogenic stimuli. Previous in vivo observations in X-SCID patients with mixed chimerism who underwent transplantation revealed that in 3 of 13 patients host B cells could cooperate with donor T cells to fully mature into immunoglobulin-producing cells.38 This suggested that at least some IL2RG mutations are compatible with normal B-cell function. In our patient, terminal B-cell differentiation was impaired and apart from antirubella antibodies he did not produce specific antibodies although the autologous revertant T cells appeared fully functional. These data indicate an intrinsic defect of the patient's B cells in vitro and in vivo.
From a clinical point of view, the most important observation was that the revertant T-cell progenitor provided our patient with significant immunity. He had the phenotype of a very mild immunodeficiency with recurrent bronchitis as its main manifestation. In the context of borderline hypogammaglobulinemia and failure to produce specific antibodies, this clinical picture was more suggestive of common variable immunodeficiency than of SCID. It is well known that patients with point mutations in What is the prognosis for our patient and for other patients with primary immunodeficiencies who have a milder clinical course due to genetic reversions? P1, who had a similar immunologic profile (Table 1), initially presented with interstitial pneumonia and a bacillus Calmette-Guérin (BCG) skin abscess at 6 months of age. On intravenous immunoglobulin (IVIG) and antibiotic prophylaxis, he had no severe infections between 2 and 4 years of age. After that, he developed chronic eczema, episodes of prolonged diarrhea, and recurrent respiratory tract infections leading to bronchiectasis and clubbing. At the age of 6 years, the lung disease significantly deteriorated and he received a cord blood transplant after myeloablative conditioning at 6 years, 11 months of age. He is currently 15 years of age and well with moderately reduced lung function. In that patient, T-cell repertoire stability was demonstrated between 3 and 5 years.16 Unfortunately, a close immunologic follow up was not performed thereafter, when the clinical course deteriorated. For P2, a matched sibling donor is not available, but a matched unrelated hematopoietic stem cell transplant donor has been identified. However, under subcutaneous immunoglobulin (SCIG) therapy this patient is presently in perfect health with no more significant episodes of bronchitis. Together with the family we have therefore decided not to perform hematopoietic stem cell transplantation (HSCT) at this time point. Overall, there is currently insufficient information to answer the important question of whether the T-cell repertoire generated by revertant precursors can be sufficient to provide immunologic protection in the long term. Careful immunologic surveillance will be essential to evaluate the longevity and functionality of the life-saving genetic revertant in our patient.
Contribution: C.S. performed experiments and wrote the paper; U.P. and K.S. performed genetic analysis; E.W. performed CDR3 spectratyping; P.F. performed CDR3 spectratyping analysis; W.F. performed SCT in P1 and provided follow-up information on P1; T.N. provided follow-up information on P1; K.G. performed STAT5/5 phosphorylation assays; K.B. analyzed skewed X inactivation; M.S. performed B-cell phenotyping; H.E. performed structure modeling of IL2R; J.R. performed experiments; A.S.-F. helped in discussion and interpretation of genetic results; U.G.-W. provided clinical care of P2 and provided patient samples; and S.E. designed experiments and wrote the paper. Conflict-of-interest disclosure: The authors declare no competing financial interests. Correspondence: Stephan Ehl, Center for Pediatrics and Adolescent Medicine, Mathildenstr. 1, 79106 Freiburg, Germany; e-mail: stephan.ehl{at}uniklinik-freiburg.de.
We are very grateful to the patient and his family for their cooperation. Excellent technical assistance was provided by F. Seifert, S. Braun, J. Janz, and G. Keller. We are grateful to C. Struck for support in the graphic display of spectratyping data. This work was supported by the Deutsche Forschungsgemeinschaft (SFB620 TPA4 [S.E.] and Z1 [P.F.]).
Submitted April 24, 2008; accepted August 10, 2008.
Prepublished online as Blood First Edition Paper, August 26, 2008
DOI: 10.1182/blood-2008-04-153361
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Abstract
Introduction
C transition in exon 3 at nucleotide 466 was detected. Interestingly, sequence analysis of DNA derived from PBMCs showed a dual signal with about 40% wild-type and 60% mutated sequence. After presence of maternal cells was excluded by STR analysis, we extracted DNA from sorted lymphocyte subpopulations and a buccal swab probe. Wild-type sequence was detected in all 
) and median and range from healthy controls as determined by flow cytometry.
