An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation.
The X-linked hyper-IgM syndrome (XHIGM, OMIM # 308230) is a rare, inherited immune deficiency disorder characterized by recurrent infections associated with low IgG and IgA and normal to increased IgM serum levels. XHIGM is caused by defects in the CD40LG/TNFSF5 gene, encoding for CD40 ligand (CD40LG) (OMIM#300386), a molecule predominantly expressed by activated CD4+ T lymphocytes . It interacts with CD40 (OMIM#109535) molecule expressed by B lymphocytes and monocytes. Loss of interaction between them results in impairment of terminal B lymphocyte differentiation, monocyte activation, and T lymphocyte priming .
XHIGM patients have severe clinical features but different clinical phenotypes suggestive for combined immune deficiencies. In a report of 176 patients, 80% of patients came to medical attention due to recurrent upper and lower respiratory tract infections, 40% had varied gastrointestinal manifestations, and 11% of patients had central nervous system disease . Liver disease and sclerosing cholangitis are clinical "red flags" and an important predictor of mortality in XHIGM patients similar to liver dysfunction reported to occur in a small subset of patients with common variable immunodeficiency (CVID) [1, 3].
Overall prognosis for all patients with XHIGM remains guarded, with an average of 20% survival by age 25 years . In a recent retrospective study in both transplanted or nontransplanted XHIGM patients, the median postdiagnosis survival was 25 years . Azzu V et al.  have reported that Ig replacement treated, CD40L deficient patients can live at least into the 4th decade without HSCT but that the burden of liver disease is as high as 40% in those who have not received HSCT.
In the view of the severe manifestations and outcomes associated with defects of the CD40LG/CD40 axis, hematopoietic stem cell transplantation (HSCT) has been successfully used to cure CD40LG deficiency. Since the first report in 1995 about HSCT in XHIGM, many subsequent series have been published, demonstrating improved survival and success of this therapeutic modality . However, in recent years there are a few case reports showing that median survival time is similar for patients treated with or without HSCT. In this case report, we would like to present a 30year-old XHIGM patient who has been followed up for 23 years with regular intravenous immunoglobulin and without HSCT and with no severe and opportunistic infection. In addition, we aimed to review the best treatment options to increase survival rate and quality of life for XHIGM patients.
2. Case Presentation
The male patient is the second child of nonconsanguineous, healthy parents and the first child is female and healthy. He was admitted to our hospital with recurrent upper and lower respiratory tract infections and recurrent otitis media when he was 7 years old. His initial immunologic evaluation revealed low IgG (307 mg/dl, normal: 1040 [+ or -] 203 mg/dl), normal IgA (112 mg/dl, normal: 108 [+ or -] 42 mg/dl), and normal to borderline IgM levels (122 mg/dl, 97 [+ or -] 42 mg/dl). He had normal numbers of CD3+ T cells (61%, 3660/[mm.sup.3]) and CD19+ B cells (20%, 1200/[mm.sup.3]) and normal numbers and percentages of other lymphocyte phenotypes (CD3+CD4+ T helper cells 29% and 1740/[mm.sup.3], CD3+CD8+ T cytotoxic cells 28% and 1680/[mm.sup.3], CD3-CD16+CD56+ natural killer cells 16% and 960/[mm.sup.3]). Specific IgG antibodies against tetanus and hepatitis B vaccines were both undetectable. In chest CT, he had a very mild bronchiectasis in left lower lobe of the lungs. His other laboratory tests including leukocyte, lymphocyte, haemoglobin counts, liver and kidney function tests, serologic investigations for common viruses, autoantibodies such as antinuclear antibody, direct Coombs tests, and abdominal ultrasonography were all normal. The patient did not have any sign of liver disease, there was no elevation in liver biochemistry tests such as ALT (alanine transferase), GGT (gamma-glutamyl transpeptidase), and ALP (alkaline phosphatase), and there were no findings of biliary dilatation, sclerosing cholangitis, or cirrhotic liver in ultrasound and abdominal computerized tomography. Cryptosporidium parvum was not detected in many stools of patient.
He was initially diagnosed as common variable immunodeficiency (CVID) and we began to give him intravenous immunoglobulin (IVIG) replacement therapy (0.5 gm/kg) with four-week intervals. During follow-up under IVIG therapy, he was extremely well and had never severe infections. He had once or twice slight pharyngitis in a year and his school attendance was excellent.
During follow-up for 22 years until last year, his IgG values just before IVIG therapies were between 500 and 600 mg/dl. IgM and IgA values were between 90 and 133 mg/dl and 70 and 104 mg/dl, respectively. When he was 20 years old, genetic analyses for TACI (TNFRSF13B), APRIL (TNFSF13), ICOS (inducible T cell costimulator), and CD19 were performed and no disease causing mutations were detected in these genes known to be associated with CVID.
No more investigations were performed until 2017 and the patient still had the diagnosis of CVID and he had no severe health problems. In 22 years, he had only once easily treated bronchitis and his bronchiectatic area in the left lower lobe also recovered a few years after the diagnosis.
In 2017, we decided to perform "targeted next generation sequencing (TNGS)" in order to understand his molecular pathology. TNGS workflow based on an Ion AmpliSeq[TM] Primary Immune Deficiency Research Panel was designed for sequencing 264 PID genes on Ion S5[TM] Sequencer. A hemizygous c.31C>T(p.Arg11Ter) mutation was found in CD40LG gene. This mutation has been described before and found in CD40LG database. PCR amplification and Sanger sequencing were performed to verify the segregation of the mutation in CD40LG among the family members. The mother was heterozygous carrier for this mutation and his sister did not have any mutation in CD40LG gene (Figure 1).
Then, the patient has been examined again for flow cytometric tests and lymphocyte subsets were found to be normal again. In order to detect T cell activation and CD40LG expression, peripheral blood mononuclear cells were stimulated with phorbol 12-myristate 13-acetate (PMA, 20ng/ml) and ionomycin (1M) for 4 hours. The following antibody and fusion proteins were used: anti-CD40LG mAb (clone 89-76, BD biosciences, Belgium, and clone 24-31, BioLegend, CA). CD69 upregulation on CD3+ T cells stimulated with PMA and ionomycin was found to be 99.2% after stimulation while it was 1.3 before stimulation, and this finding showed us that T imphocytes were highly activated. In CD3+ T lymphocytes gate, CD8-CD154+ cells were 16,9% after stimulation while they were 5.1% before stimulation.
This finding showed us that this mutation in CD40LG gene resulted in highly decreased, but not absent, CD40LG expression.
After XHIGM diagnosis, we did not change his treatment regimen. The patient did not accept to use subcutaneous immunoglobulin therapy, told the clinicians that his quality of life is very well on IVIG, and decided to marry in September 2018. In agreement with him, we have never thought about HSCT for this patient because of probable life-threatening risks of HSCT.
We reported a 30-year-old male with low serum IgG and with normal serum IgA and IgM and recurrent infections before IVIG therapy. Absolute and relative numbers of lymphocyte subsets were normal, excluding the diagnosis of an X-linked agammaglobulinemia (Bruton's disease). Despite normal IgM levels, XHIGM was diagnosed after follow-up of 23 years. A literature search revealed that approximately 6.4% of X-HIGM patients had been found to have low to normal serum IgM levels . Winkelstein et al.  reported eight cases and Gilmour et al.  reported four cases with low IgM, n: 8/56 and 4/17, respectively. Different studies in literature showed that many patients with low to normal serum IgM levels may not have undergone diagnostic procedures for XHIGM . The first message for this case report has to be as follows: diagnostic delay has been noted as a clinical problem for patients with CD40LG deficiency, with up to 50% of patients presenting with low or normal IgM levels, so that all the hypogammaglobulinemic patients, not only with high serum IgM levels, but also with normal to low IgM levels, have to be examined for CD40LG expression on activated T lymphocytes.
Although most patients present with XHIGM during childhood, the age at presentation can be as late as the fifth decade of life . Although our patient was admitted to Pediatric Immunology Clinic at seven years of age, the exact diagnosis could be reached after we began to perform TNGS assay when he was 29 years old. Female carriers have been reported as showing variable expression of CD40LG on activated T cells. As low as 32% of activated T cells expressing CD40LG can be seen in asymptomatic carriers . Our patient's CD40LG expression was less than the carriers' levels.
Mutations in CD40LG gene are highly heterogenous. CD40LG database contained more than 250 public entries . Besides more mutations on CD40LG were reported in other studies . Considering the published results, the common type of mutations in the CD40LG might be missense mutations, followed by deletion/insertion mutations, nonsense mutations, and splice-site mutations . Nonsense mutations like our patient's mutation in the CD40LG database differed between 10.5% and 26.9% in a cohort analysis of all reported different mutations . Various mutations reflected the heterogeneity of not only genotypes, but also phenotypes. Our patient was receiving immunoglobulin therapy and trimethoprim/sulfamethoxazole on a continuous basis and never had severe complications, such as lung disease or opportunistic infections. We suggest that this clinical phenotype was highly related to the type of the mutation observed in our patient, because we still need further progress in better understanding of the molecular heterogeneity and clinical correlations associated with this uncommon disorder.
Azzu V et al.  found a higher prevalence of liver disease (33%) in XHIGM patients compared with most other studies, approximately 20% in data from a European registry and 6% in two US registries. In CVID patients, a recent study found liver disease in 5% of a cohort of 261 patients . Azzu et al.  have reported that estimates from their cohort of over 100 adult CVID patients indicated a greater proportion of patients who have liver disease related to their primary immunodeficiency. XHIGM patients with liver disease had statistically significant elevations in liver chemistry, abnormal liver imaging including cirrhotic livers, biliary dilatation, or sclerosing cholangitis associated with Cryptosporidium and cytomegalovirus infection. Our patient did not have any clinical and laboratory signs of liver disease and also imaging studies including ultrasonography were all normal. On the other hand, in Azzu et al.'s study , crude mortality was higher in liver disease group (38%) compared with the group without liver disease (6%). Kaplan-Meier log-rank analysis showed decreased survival in XHIGM patients with liver disease .
The risk in the HSCT treated XHIGM patients decreased in the past two decades and those patients treated with HSCT had better scores that measured general well-being and activities of the daily life . Early age at transplantation and absence of liver disease were associated with best survival . Azzu et al.  have reported that early HSCT before age of 10 years was performed in patients without liver disease and survival was excellent. A report on HSCT for 38 XHIGM patients showed that 58% of the patients were cured, but 32% died of infection-related complications such as severe cryptosporidiosis and graft-versus-host disease . From a recent report of 175 XHIGM patients collected from both US and European data, 56 of 67 subjects who underwent HSCT have survived. The median survival time was similar for transplanted and nontransplanted subjects in this cohort . A report of 56 XHIGM patients in Japan showed greater overall survival rates in HSCT recipients, with significantly event-free and disease-free survival rates in patients younger than 5 years at the time of the transplant . As a result, it seems that XHIGM patients who have potential HSCT donors, HSCT performed in the first decade and before the development of liver diseases, might offer not only a survival advantage, but also improved long-term general well-being. For those patients who do not have the option of HSCT, it is encouraging to see that long-term survival has improved in the last 4 decades .
In 2018, many questions remain. Does transplantation prevent the appearance of malignancy? How are transplant related morbidities, including graft failure and GVHD, impacting a patient's quality of life? Will gene therapy and recombinant CD40LG therapy be better options in the future? Long-term studies on the benefit and risk of HSCT versus immunoglobulin replacement therapy and P (carinii) jiroveci prophylaxis need to be done to determine the best course of action for a particular patient.
This case report underlines the fact that CD40LG mutations leading to immunoglobulin class switch defects are showing enormous interpatient variations regarding serum IgM levels, CD40LG levels on activated T cells, age at diagnosis, severity of clinical findings, and follow-up therapies with or without HSCT.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
 M. T. de la Morena, "Clinical phenotypes of hyper-IgM syndromes," The Journal of Allergy and Clinical Immunology: In Practice, vol. 4, no. 6, pp. 1023-1036, 2016.
 M. T. de la Morena, D. Leonard, T. R. Torgerson et al., "Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation," The Journal of Allergy and Clinical Immunology, vol. 139, no. 4, pp. 1282-1292, 2017.
 V. Azzu, J. E. Elias, A. Duckworth et al., "Liver transplantation in adults with liver disease due to common variable immunodeficiency leads to early recurrent disease and poor outcome," Liver Transplantation, vol. 24, no. 2, pp. 171-181, 2018.
 J. A. Winkelstein, M. C. Marino, H. Ochs et al., "The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients," Medicine, vol. 82, no. 6, pp. 373-384, 2003.
 V. Azzu, L. Kennard, B. Morillo-Gutierrez et al., "Liver disease predicts mortality in patients with X-linked immunodeficiency with hyper-IgM but can be prevented by early hematopoietic stem cell transplantation," The Journal of Allergy and Clinical Immunology, vol. 141, no. 1, pp. 405-408.e7, 2018.
 K. Mitsui-Sekinaka, K. Imai, H. Sato et al., "Clinical features and hematopoietic stem cell transplantations for CD40 ligand deficiency in Japan," The Journal of Allergy and Clinical Immunology, vol. 136, no. 4, pp. 1018-1024, 2015.
 A. Heinold, B. Hanebeck, V. Daniel et al., "Pitfalls of "hyper" IgM syndrome: A new CD40 ligand mutation in the presence of low IgM levels. A case report and a critical review of the literature," Infection, vol. 38, no. 6, pp. 491-496, 2010.
 K. C. Gilmour, "Immunological and genetic analysis of 65 patients with a clinical suspicion of X linked hyper-IgM," Molecular Pathology, vol. 56, no. 5, pp. 256-262, 2003.
 N. C. Gunaydin, J. Chou, N. E. Karaca et al., "A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity," Clinical Immunology, vol. 153, no. 2, pp. 288-291, 2014.
 D. Hollenbaugh, L. H. Wu, H. D. Ochs et al., "The random inactivation of the X chromosome carrying the defective gene responsible for X-linked hyper IgM syndrome (X-HIM) in female carriers of HIGM1," The Journal of Clinical Investigation, vol. 94, no. 2, pp. 616-622, 1994.
 L. Wang, W. Zhou, W. Zhao et al., "Clinical Features and Genetic Analysis of 20 Chinese Patients with X-Linked Hyper-IgM Syndrome," Journal of Immunology Research, vol. 2014, Article ID 683160,12 pages, 2014.
 I. J. Fuss, J. Friend, Z. Yang et al., "Nodular regenerative hyperplasia in Common Variable Immunodeficiency," Journal of Clinical Immunology, vol. 33, no. 4, pp. 748-758, 2013.
 E. A. Leven, P. Maffucci, H. D. Ochs et al., "Hyper IgM Syndrome: a Report from the USIDNET Registry," Journal of Clinical Immunology, vol. 36, no. 5, pp. 490-501, 2016.
 N. Qamar and R. L. Fuleihan, "The hyper IgM syndromes," Clinical Reviews in Allergy & Immunology, vol. 46, no. 2, pp. 120-130, 2014.
Necil Kutukculer, (1) Neslihan Edeer Karaca, (1) Guzide Aksu, (1) Ayca Aykut, (2) Erhan Pariltay, (2) and Ozgur Cogulu (2)
(1) Ege University Faculty of Medicine, Department of Pediatric Immunology, Izmir, Turkey
(2) Ege University Faculty of Medicine, Department of Medical Genetics, Izmir, Turkey
Correspondence should be addressed to Necil Kutukculer; email@example.com
Received 31 July 2018; Revised 16 September 2018; Accepted 20 September 2018; Published 14 October 2018
Academic Editor: Alessandro Plebani
Caption: FIGURE 1: (a) Targeted next generation sequencing analysis in genomic DNA of patient. A nonsense mutation in Exon 1 (c.31C>T) changes an arginine (R) codon (CGA) into a translation termination (X) codon (TGA) at amino acid position 11 (p.ArgllTer). (b) Sanger sequencing analysis in genomic DNA of patient. (c) The mother was heterozygous carrier and the sister had wild type gene sequences.
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|Title Annotation:||Case Report|
|Author:||Kutukculer, Necil; Karaca, Neslihan Edeer; Aksu, Guzide; Aykut, Ayca; Pariltay, Erhan; Cogulu, Ozgur|
|Publication:||Case Reports in Immunology|
|Date:||Jan 1, 2018|
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