key: cord-0943292-xxs7oiwx
authors: Alsum, Zobaida; AlZahrani, Mofareh S.; Al-Mousa, Hamoud; Alkhamis, Nouf; Alsalemi, Abdulkareem A.; Shamseldin, Hanan E.; Alkuraya, Fowzan S.; Alangari, Abdullah A.
title: Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in IKBKB
date: 2020-02-14
journal: Front Pediatr
DOI: 10.3389/fped.2020.00009
sha: 2f38704ef0009750d4c48d1cd7ac81e898023527
doc_id: 943292
cord_uid: xxs7oiwx

Background: Inhibitor of kappa kinase 2 (IKK2) deficiency is a recently described combined immunodeficiency. It undermines the nuclear factor-kappa B (NF-κB) activation pathway. Methods: The clinical and immunological data of four patients diagnosed with combined immunodeficiency (CID) from two related Saudi families were collected. Autozygosity mapping of all available members and whole exome sequencing of the index case were performed to define the genetic etiology. Results: The patients had early onset (2–4 months of age) severe infections caused by viruses, bacteria, mycobacteria, and fungi. They all had hypogammaglobulinemia and low absolute lymphocyte count. Their lymphocytes failed to respond to PHA mitogen stimulation. A novel homozygous non-sense mutation in the IKBKB gene, c.850C>T (p. Arg284*) was identified in the index patient and segregated with the disease in the rest of the family. He underwent hematopoietic stem cell transplantation (HSCT) from a fully matched sibling with no conditioning. The other three patients succumbed to their disease. Interestingly, all patients had delayed umbilical cord separation. Conclusion: IKK2 deficiency causes CID with high mortality. Immune reconstitution with HSCT should be considered as early as possible. Delayed umbilical cord separation in CID patients may be a clue to IKK2 deficiency.

Nuclear factor-kappa B (NF-kB) is a transcription factor that plays a major role in various biological processes including the immune system development, activation, and regulation. This transcription factor complex is held inactive in the cytoplasm by the inhibitor of NF-kB (IκB). The classical activation pathway of NF-kB is triggered by a large number of extracellular stimuli through different receptors, which result in the phosphorylation of IκB by IκB kinase (IKK complex; IKKα, IKKβ/IKK2, and IKKγ/NEMO) and the subsequent release of NF-kB complex so it can translocate into the nucleus and drive target gene expression (1) .

Different primary immunodeficiency disorders result from genetic defects that involve components linked to the NF-kB activation pathway (2) . IKK2 deficiency is a recently described combined immunodeficiency disease that leads to impairment of NF-kB signaling (3) . Affected patients develop early severe and recurrent infections caused by bacterial, viral, fungal, and mycobacterial organisms. Unlike patients with IKKα and IKKγ mutations, IKK2-deficient patients do not typically have ectodermal dysplasia. Indeed, out of 22 patients with IKK2 deficiency described in the literature, only one patient has ectodermal dysplasia in the form of conical teeth (3) (4) (5) (6) (7) .

Herein, we describe the clinical manifestations and the immunologic features of four Saudi patients from two related families with a diagnosis of combined immunodeficiency due to novel homozygous non-sense mutation in IKBKB.

The medical records of four Saudi patients from two related families with a diagnosis of combined immunodeficiency were reviewed. The clinical and immunological data were collected. Autozygosity mapping of all available members and whole exome sequencing of the index member were performed as previously described (8) . Written consent was obtained from 

Our patients (V:1, V:2, V:5, and V:8) belong to two related Saudi families ( Figure 1A) . They had early onset (2-4 months of age) severe infections caused by viruses, bacteria, mycobacteria, and fungi. The organisms include Klebsiella pneumonuia, Candida albicans, CMV, and BCG ( Table 1) , which were associated with different clinical manifestations ( Table 1) . Interestingly, all four patients had delayed umbilical cord separation at 2 months. They all displayed hypogammaglobulinemia. Where data is available, they had low absolute lymphocyte count (420-2,680 cells/mm 3 ), and their lymphocytes failed to respond to PHA mitogen ( Table 1) . A novel homozygous non-sense mutation in the IKBKB gene, c.850C>T (p. Arg284 * ) (Figures 1B,C) was identified in patient V:5 within the candidate autozygome, and Sanger sequencing confirmed its segregation with the disease in the remaining living siblings and parents (Figures 1A,B) . Three patients (V:1, V:2, and V:8) succumbed to their disease's infectious complications before commencing hematopoietic stem cell transplantation (HSCT).

Patient V:5 underwent HSCT from a fully matched sibling (10/10) at 19 months of age. To save his life and because of the disseminated BCGitis, he received no conditioning and no GVHD prophylaxis. The CD34 dose was 9.2 × 10 6 /kg. He 

This is the largest cohort of IKK2 deficiency reported in the Saudi population. In general, the clinical features of our patients were not different from previously reported cases. Susceptibility to a wide range of infections caused by opportunistic and nonopportunistic organisms were commonality. The generalized maculopapular rash, hepatosplenomegaly, chorioretinitis, and CNS complications in our patients are probably related to the chronic CMV and disseminated BCG infections. All reported patients succumbed to their disease during infancy unless they had successful HSCT ( Table 2) . On average, the degree of lymphopenia was more profound in our patients (420-2,680/mm 3 ) compared to others (1,520-11,850/mm 3 ) (7). Interestingly, all our patients had delayed umbilical cord separation [normal separation occurs in 1-2 weeks (8)] Patient V:6, who died in infancy from a febrile illness before diagnosis and the identification of the genetic defect in the family, was also reported to have had delayed separation of the umbilical cord. None of the reported patients with IKK2 deficiency had delayed cord separation except one from Saudi Arabia, but with a different mutation (3) (4) (5) (6) (7) . No neutrophil chemotaxis or adhesion assay was done for the patients. Delayed cord separation was reported in conditions that affect neutrophil number and/or compromise their function including leukocyte adhesion defects as well as MyD88 and IRAK4 deficiency, which are upstream to the NF-κB activation pathway (9) (10) (11) (12) . This feature may be a clue to IKK2 deficiency in patients with combined immunodeficiency. The mechanism by which IKBKB mutation may predispose to delayed cord separation is not clear. It has been reported that neutrophil infiltration was prominent during the cord separation process in healthy babies, and a defect in neutrophil chemotaxis and adhesion was illustrated in cases of leukocyte adhesion deficiency (13) . Since all IKK2 deficiency patients in the literature did not exhibit delayed cord separation except one Saudi patient with a different mutation, it is likely that this feature is a result of a complex interaction between the IKBKB defect and other modifier genes. On the other hand, a gain-of-function (GOF) mutation in IKBKB leads to a relatively mild form of combined immunodeficiency, ectodermal dysplasia, and immune dysregulation, where affected patients may live to their fourth decade. Although both diseases result in hypogammaglobulinemia and lymphopenia, patients with IKBKB GOF mutation have lower number of naïve T lymphocytes with overactivated memory cells (14) .

In our index patient, his unstable clinical condition and the disseminated BCGitis dictated the decision of non-conditioned HSCT. The fact that he had a sustained lymphoid engraftment without conditioning is likely due to the severe T-cell dysfunction in this type of immunodeficiency. We do not have a clear explanation why our index case did not clear the disseminated BCGitis inspite of the recovered in vitro lymphoproliferative response to PHA. One possibility is that the donor cells are anergic to BCG, but we could not test for that. So far, 13 out of 27 patients with IKK2 deficiency including our cohort had undergone HSCT. Only five were alive at the time of reporting, while those who did not receive HSCT succumbed to their disease in their infancy or early childhood. All survivors received myeloablative conditioning except our patient, while the remaining eight patients received non-myeloablative conditioning (n = 5), reduced intensity conditioning (n = 1), or no conditioning (n = 2) (14) . Although it is difficult to draw a conclusion from such limited number of reported patients, it seems that no conditioning or reduced intensity conditioning are not sufficient to cure the disease, and myeloablative protocol is needed to establish a good immune reconstitution.

All datasets generated for this study are included in the article/supplementary material.

The studies involving human participants were reviewed and approved by The Research Advisory Council (RAC) at King Faisal Specialist Hospital and Research Center (RAC# 2121053). Written informed consent to participate in this study was provided by the participants' legal guardian/next of kin.

NF-kappaB: two sides of the same coin

Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling

Deficiency of innate and acquired immunity caused by an IKBKB mutation

Immunodeficiency and disseminated mycobacterial infection associated with homozygous nonsense mutation of IKKβ

Immunodeficiency associated with a nonsense mutation of IKBKB

A nonsense mutation in IKBKB causes combined immunodeficiency

Clinical presentation, immunologic features, and hematopoietic stem celltransplant outcomes for IKBKB immune deficiency

The application of next-generation sequencing in the autozygosity mapping of human recessive diseases

The time of separation of the umbilical cord

Infantile hemophagocytic lymphohistiocytosis in a case of chediakhigashi syndrome caused by a mutation in the LYST/CHS1 gene presenting with delayed umbilical cord detachment and diarrhea

Infectious diseases in patients with IRAK-4, MyD88, NEMO, or IκBα deficiency

A novel truncating mutation in MYD88 in a patient with BCG adenitis, neutropenia and delayed umbilical cord separation

Invasive bacterial infection in patients with interleukin-1 receptor-associated kinase 4 deficiency

Gain-of-function IKBKB mutation causes human combined immune deficiency

ZA acquired data and wrote the manuscript. FA and HS designed and conducted the genetic study. HA-M contributed to writing the transplantation and post transplantation part of the manuscript. MA, NA, and AAls substantially contributed to the acquisition and analysis of the clinical data for the work. AAla acquired data, supervised, critically revised and edited the work for intellectual content. All authors provided approval for publication of the content and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. 

An abstract of this manuscript was presented in the European Society of Immunodeficiency (ESID) 2017 conference. They kindly granted permission to publish this manuscript.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.The reviewer SP declared a past co-authorship with the author HA-M to the handling editor.Copyright © 2020 Alsum, AlZahrani, Al-Mousa, Alkhamis, Alsalemi, Shamseldin, Alkuraya and Alangari. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.