Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage

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Science  15 Nov 2013:
Vol. 342, Issue 6160, pp. 866-871
DOI: 10.1126/science.1243292

Answers from Exomes

Exome sequencing, which targets only the protein-coding regions of the genome, has the potential to identify the underlying genetic causes of rare inherited diseases. Angulo et al. (p. 866, published online 17 October; see Perspective by Conley and Fruman) performed exome sequencing of individuals from seven unrelated families with severe, recurrent respiratory infections. The patients carried the same mutation in the gene coding for the catalytic subunit of phosphoinositide 3-kinase δ (PI3Kδ). The mutation caused aberrant activation of this kinase, which plays a key role in immune cell signaling. Drugs inhibiting PI3Kδ are already in clinical trials for other disorders.


Genetic mutations cause primary immunodeficiencies (PIDs) that predispose to infections. Here, we describe activated PI3K-δ syndrome (APDS), a PID associated with a dominant gain-of-function mutation in which lysine replaced glutamic acid at residue 1021 (E1021K) in the p110δ protein, the catalytic subunit of phosphoinositide 3-kinase δ (PI3Kδ), encoded by the PIK3CD gene. We found E1021K in 17 patients from seven unrelated families, but not among 3346 healthy subjects. APDS was characterized by recurrent respiratory infections, progressive airway damage, lymphopenia, increased circulating transitional B cells, increased immunoglobulin M, and reduced immunoglobulin G2 levels in serum and impaired vaccine responses. The E1021K mutation enhanced membrane association and kinase activity of p110δ. Patient-derived lymphocytes had increased levels of phosphatidylinositol 3,4,5-trisphosphate and phosphorylated AKT protein and were prone to activation-induced cell death. Selective p110δ inhibitors IC87114 and GS-1101 reduced the activity of the mutant enzyme in vitro, which suggested a therapeutic approach for patients with APDS.

Respiratory infections are the most common illnesses of people worldwide. Recurrent respiratory infections may lead to bronchiectasis, a permanent, abnormal dilation of bronchi (1). Susceptibility to recurrent respiratory infections and bronchiectasis may be conferred by an underlying primary immunodeficiency (PID) (1, 2). PIDs have variable penetrance, and those that have a milder course may remain undiagnosed. Mutations in more than 200 genes are known to cause various PIDs (3). Recent improvements in DNA sequencing technology provide an opportunity to study the patient’s whole genome or its coding part, known as the exome (4). This technological advancement has improved the genetic diagnostics of PIDs in patients with recurrent and severe infections and facilitated the identification of novel causative genes and mutations.

We used exome sequencing to search for causative mutations in 35 PID patients from the United Kingdom who suffered recurrent infections and had a family history of susceptibility to infections (5). After identification of genetic variants in these patients, we excluded common polymorphisms previously detected in the 1000 Genomes and National Heart, Lung, and Blood Institute (NHLBI) projects (table S1) (5). When cross-checking the remaining rare variants, we noted that three patients from one family (P1, P2, and P3 in family A) and one patient from another family (P5 in family B) had the same heterozygous G to A mutation at position 9,787,030 on chromosome 1, c.3061G>A in the PIK3CD gene (Fig. 1). This mutation was not present in the other exomes and was the only rare variant shared among all patients in these two unrelated families. It encodes an amino-acid substitution, a glutamic acid for a lysine, at position 1021 (E1021K) of the p110δ protein, the catalytic subunit of phosphoinositide 3-kinase δ (PI3Kδ). Sanger sequencing confirmed the presence of the E1021K mutation in these patients and four additional affected family members. In both families, the mutation cosegregated with the clinical phenotype (Fig. 1).

Fig. 1 Families with the E1021K p110δ mutation.

(A) Open circles and squares, unaffected; filled circles and squares, affected; partly filled circles and squares, available data indicate recurrent infections. Age at the time of death is shown for patients who died ≤30 years of age. PIK3CD genotype is shown if known. wt, wild-type allele encoding glutamic acid (E1021); mut, mutant allele encoding lysine (K1021). (B) Sequence chromatogram showing heterozygous mutation c.3061G>A in the PIK3CD gene leading to the E1021K amino acid change in p110δ. CpG dinucleotide is underlined.

We then designed a genotyping assay for this E1021K mutation and screened 3346 healthy subjects, including 2296 from the United Kingdom and 1050 representing 51 different populations from around the world (5). No healthy carriers of E1021K were identified in these two large cohorts, supporting our hypothesis that this is a pathogenic mutation rather than a rare neutral polymorphism. We then studied DNA samples of an additional heterogeneous cohort of 134 PID patients from the United Kingdom and Ireland (5). In this cohort, we identified five further patients from three unrelated families (C, D, and E) who had the same heterozygous E1021K mutation (Fig. 1A). The apparent high frequency of the mutation among PID patients and the fact that P8 (family C) had previously been diagnosed with hyper-immunoglobulin M (hyper-IgM) syndrome prompted us to study an additional cohort from France comprising 15 hyper-IgM patients from 13 families that had previously undergone exome sequencing. Among these, we found three patients from two unrelated families, F and G, with the same mutation, indicating that E1021K may cause a typical hyper-IgM syndrome. One additional patient was identified among family members, bringing the overall number of patients with the E1021K mutation to 17.

Sequencing of the healthy parents of P8 in family C showed that both were homozygous for the normal allele (Fig. 1A). Genome-wide identity-by-descent analysis in family C confirmed the relationship of both parents to P8, thus classifying this E1021K mutation as de novo. The mutation was present in DNA isolated from both fibroblast and blood samples of P8 and therefore is likely to be germline, rather than somatic. Then, in families A to E, we studied genotypes of 149 markers in a 2-Mb interval on chromosome 1 flanking the mutation (5). We found no shared long-range haplotypes across any pair of families and no flanking markers that were consistently in linkage disequilibrium with the mutation across all five families. These data strongly suggest a recurrent mutation, rather than a founder effect. Nucleotide G in position 9,787,030 is part of a CpG dinucleotide (Fig. 1B) that is known to be ~30 times more prone to transition mutations (e.g., G>A) than an average nucleotide in the genome (6).

Before our genetic analysis, patients from families A to G were not considered to have the same disease etiology. The discovery of the same causative mutation in these patients prompted us to compare their clinical and immunological histories (table S2), revealing the phenotype of this PID, which is characterized by recurrent respiratory infections and progressive airway damage (Table 1, supplementary text, and figs. S1 and S2). Whereas the immunological phenotype was largely consistent between patients, the clinical presentation and disease course have been variable (e.g., mild disease in P10) (table S2). Such clinical variability may be explained by differences in lifestyle, exposure to pathogens, treatment efficacy, and possibly by modifying genetic factors.

Table 1 Summary of clinical and immunological features of patients with the E1021K p110δ mutation.

CT, computed tomography; HSV, herpes simplex virus; CMV, cytomegalovirus; VZV, varicella-zoster virus; EBV, Epstein-Barr virus.

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To understand how the E1021K mutation caused immunodeficiency, we first studied its effect on p110δ function. The p110δ protein is a catalytic subunit that, together with a regulatory subunit, forms PI3Kδ, a heterodimeric lipid kinase. PI3Kδ phosphorylates phosphatidylinositol 4,5-bisphosphate (PIP2), generating phosphatidylinositol 3,4,5-trisphosphate (PIP3), an important second messenger molecule. We cloned the cDNA of p110δ and introduced the E1021K change by site-directed mutagenesis. Subsequently, we expressed both normal and mutant p110δ proteins, together with the regulatory subunit p85α, in baculovirus-infected insect cells and purified the proteins (fig. S3A). We measured lipid kinase activity using a modified membrane capture assay (7) and found that the basal PIP3 production by PI3Kδ containing the mutant p110δE1021K subunit was higher by up to a factor of 6 than that produced by the wild-type PI3Kδ (Fig. 2A and fig. S3B). After stimulation with a platelet-derived growth factor (PDGF) receptor’s bis-phosphorylated peptide (pY), the activity of both wild-type and mutant PI3Kδ increased, but PIP3 production by the mutant PI3Kδ was still up to 3 times as high (Fig. 2A and fig. S3C). We used two structurally related isoform-selective PI3Kδ inhibitors, IC87114 and GS-1101 (8, 9), and found that both reduced the activity of the mutant PI3Kδ as efficiently as that of the wild-type PI3Kδ (Fig. 2B), suggesting that these compounds may be effective in patients with the E1021K mutation.

Fig. 2 In vitro activity and structure of p110δ.

(A) Basal and pY-stimulated PI3K activity at 20-nM concentration. Graphs are mean ± SD of three independent experiments. P values were calculated by a two-tailed t test. (B) Inhibition of mutant and wild-type p110δ/p85α as a function of IC87114 or GS-1101 concentration (data are mean ± SD, N = 3 experiments). (C) Domain organization of p110δ. (D) Structural model of the p110δ/p85α heterodimer. p110δ catalytic subunit (pale green); nSH2 and iSH2 domains of the p85 regulatory subunit (cyan); cSH2 domain (magenta); p110δ activation loop (thick chocolate tube beneath kα12); residue E1021 of p110δ (green spheres); and the analogous residue in H1047R mutant of p110α (cyan spheres). The IC87114 inhibitor bound in the active site is shown in stick representation. (E) Membrane binding of p110δ. FRET between the PI3K complex and Dansyl-PS–containing membrane vesicles in the absence (solid lines) or presence (dashed lines) of the pY peptide (data are mean ± SD, N = 3 experiments).

To understand the mechanism by which E1021K increases PI3Kδ activity, we first modeled the structure of the mutant p110δ protein (5). p110δ is organized similarly to other PI3K catalytic subunits (Fig. 2C) (10, 11). The E1021K mutation is located in the C lobe of the kinase domain that interacts with cellular membrane, accommodates lipid substrate, and binds the cSH2 domain of the regulatory subunit (Fig. 2D). Structural modeling showed that E1021K of p110δ is positioned similarly to the somatic mutation H1047R of another PI3K isoform, p110α, which is known to increase PI3K activity in cancer cells by enhancing its association with membranes (12, 13). Therefore, we used a protein-lipid fluorescence resonance energy transfer (FRET) assay to study interaction between lipid vesicles and either wild-type p110δ or the mutant p110δE1021K. We found that p110δE1021K has a much higher basal affinity for lipid vesicles than the wild-type p110δ (Fig. 2E). After pY stimulation, the affinity of p110δE1021K was also increased, although the difference with respect to the pY-activated wild-type p110δ was less striking (Fig. 2E). These results suggest that stronger binding to membranes contributes to the increased activity of the mutant p110δE1021K protein. Another potential activating mechanism of E1021K may involve interaction of p110δ with the regulatory subunit p85α (14). Our structural model shows that E1021K may impair binding of p110δ to the inhibitory cSH2 domain (Fig. 2D), leading to increased PI3Kδ activity. However, it is unlikely to affect binding of another inhibitory p85α domain, nSH2 (Fig. 2D). This is consistent with our observation that pY stimulation further activates the mutant enzyme, probably by removing the nSH2 inhibition.

PI3Kδ is expressed predominantly in cells of hematopoietic lineage and is the major PI3K isoform signaling downstream of T and B cell antigen receptors (TCR and BCR), Toll-like receptors (TLRs), costimulatory molecules, and cytokine receptors in T, B, and myeloid cells (15). Therefore, we studied the activity of the mutant PI3Kδ ex vivo in patients’ leukocytes. We measured levels of PIP3 using a high-performance liquid chromatography–mass spectrometry–based assay (16) in CD4+ and CD8+ T cells isolated from fresh peripheral blood. In both T lymphocyte lineages we found consistently higher PIP3 levels in patients than in controls before stimulation and 10, 20, 30, and 60 s after stimulation (Fig. 3A). In patient cells treated with IC87114, the levels of PIP3 were significantly reduced (Fig. 3A). Furthermore, in stimulated patients’ T cells, we found increased levels of phosphorylated AKT protein, a major downstream mediator of PIP3 signaling (Fig. 3B). Levels of p110δ expression were normal in the patients’ T cells (Fig. 3B). We then cloned in a retroviral vector the wild-type p110δ, the mutant p110δE1021K, and p110δD911A with mutation D911A that inactivates the kinase domain, and transduced these constructs into T blasts isolated from the p110δ-knockout mouse (5). After stimulation, cells with p110δE1021K had more phosphorylated AKT than other cells (Fig. 3C and fig. S4). Together, these results strongly suggest that the E1021K mutation increases PI3K signaling in vivo as well as in vitro.

Fig. 3 Functional analyses of T cells in patients with APDS.

(A) Intracellular PIP3 levels in CD4+ and CD8+ T lymphocytes of patients (red squares, N = 6 subjects) and controls (blue circles, N = 5 subjects) at indicated times after stimulation with antibodies to CD3 and CD28 in the presence or absence of IC87114. The data are expressed as the ratio of the quantity of PIP3 divided by that of the internal standard (ISD) and normalized according to the cell number. The data show mean ± SEM. P values were calculated using two-way analysis of variance (ANOVA) with Bonferroni correction. (B) Representative (N = 3 experiments) Western blot showing levels of p110δ, AKT, and phospho-AKT (pAKT) proteins in CD4+ T cells isolated from fresh blood samples of a healthy control (C) and a patient (P) without stimulation (–) or after 10 min stimulation (+) with antibodies to CD3 and CD28. (C) Representative (N = 2 experiments) Western blot showing levels of p110δ, and pAKT proteins in CD4+ T cell blasts of a p110δ knockout mouse transduced with retroviral constructs expressing either green fluorescent protein (GFP) or wild-type p110δ (p110δWT) or kinase dead p110δ (p110δD911A) or p110δE1021K without stimulation (–) or after stimulation (+) with antibodies to CD3 and CD28. An expanded view of this blot is shown as fig. S4. (D) Quantification of surviving CD4+ and CD8+ T cells as indicated by percentage of cells excluding viability dye. Cells of patients (red, N = 4 subjects) and controls (blue, N = 7 subjects) were studied without stimulation and after stimulation with antibodies to CD3 and CD28 and in the presence of IC87114. Each subject was studied in triplicate. The data show mean ± SEM. P values were calculated using a two-way ANOVA with Sidak’s multiple comparisons test.

To study T cell responses, we stimulated purified CD4+ and CD8+ cells with antibodies to CD3 and CD28. Unexpectedly, we observed that both T cell lineages from patients were prone to cell death (Fig. 3D and fig. S5A). This phenomenon was reversed by the addition of IC87114 but not interleukin-2 (IL-2) (Fig. 3D and fig. S5B), suggesting that it is caused by the increased PI3Kδ activity. Cytokine production after stimulation of T cells was profoundly reduced in the patients and was not rescued by exogenous IL-2 (fig. S6), suggesting that T cell death occurs before any considerable cytokine response. However, stimulation with CytoStim, which did not induce T cell death, also led to reduced cytokine production by the patient-derived T cells (fig. S7). The propensity to activation-induced cell death (AICD) is consistent with the T cell lymphopenia found in our patients. It may relate in part to the increased proportion of T cells with an activated/memory phenotype (table S2) (17). Moreover, given that p110δ inhibitor reduces AICD of the patient-derived T cells, the activated p110δ may increase the AICD per se, possibly by enhancing TCR signaling.

In the patients’ B lymphocytes, we also found increased amounts of phosphorylated AKT, both before and after stimulation, although this analysis was complicated by enhanced protein degradation in the patient-derived cells (fig. S8). Studies in transgenic mice deficient for phosphatase and tensin homolog (PTEN), an enzyme that dephosphorylates PIP3, have shown that PI3Kδ activity, PIP3, and phosphorylated AKT suppress immunoglobulin class-switch recombination (CSR) in B cells. These mice have impaired B cell function, increased IgM, decreased IgG and IgA levels, and impaired antibody responses after immunization (1821). Immunological presentation of our patients resembles this phenotype and indicates a B cell defect. However, normal total IgG and IgA levels that were found in most of our patients suggest that CSR may be only partially affected. Nevertheless, inefficient antibody production impairs responses to Streptococcus pneumoniae and Hemophilus influenzae type B vaccinations in our patients, leading to recurrent infections with these pathogens. An increased population of circulating transitional B cells may reflect a block in late stages of B cell maturation or an enhanced death of mature B cells.

PI3Kδ is also highly expressed in neutrophils. We found that patient-derived neutrophils retained their ability to undergo a respiratory burst, degranulation, chemotaxis, and apoptosis (fig. S9). We measured PIP3 accumulation in tumor necrosis factor–α–primed neutrophils in response to N-formyl-Met-Leu-Phe (fMLP) stimulation at 6 s (a PI3Kγ-dependent response) and at 60 s (a predominantly PI3Kδ-mediated signal) (22) and found no significant difference between patients and controls in either response (fig. S9). Thus, the effect of the E1021K mutation on the PI3Kδ activity may be cell-type or stimulus-specific, or it may be compensated for by effects of other PI3K isoforms or PTEN. Nevertheless, we cannot exclude that a subtle defect in neutrophil function may contribute to the disease pathogenesis in these patients.

In summary, we have described a PID caused by a recurrent autosomal-dominant germline mutation E1021K in the PIK3CD gene that encodes p110δ. We found it in 17 patients from seven unrelated families, suggesting that it is frequent among PID patients and may explain a substantial fraction of patients with recurrent respiratory infections and bronchiectasis. Our rapid genotyping assay should facilitate screening for the E1021K mutation in existing PID and bronchiectasis cohorts, as well as new patients. The E1021K mutation was previously noted in one Taiwanese patient with recurrent respiratory infections and PID; however, its causative and pathogenic role has not been demonstrated (23). Here, we have shown that E1021K increases PI3Kδ activity, augmenting the production of PIP3 and activating the downstream AKT protein in lymphocytes. This leads to defects in T and B cell function and inefficient immune responses to bacterial pathogens, predisposing to recurrent respiratory infections and eventually to bronchiectasis. We named this disorder activated PI3K-δ syndrome (APDS).

Activation of the PI3K pathway is associated with malignant transformations, and it has been shown that overexpression of p110δ can transform cells (24). To date, only one of our APDS patients, P13, has been diagnosed with lymphoma (Table 1). Nonetheless, the oncogenic potential of PI3K up-regulation can be enhanced by additional mutations (25, 26). Therefore, APDS patients may be at increased risk of leukemia or lymphoma if they acquire additional somatic mutations.

The APDS patients described here had been treated with immunoglobulin replacement and antibiotics. Despite this, there is evidence of considerable airway damage in most cases. Because of progressive severe disease after splenectomy, patient P8 underwent allogeneic hematopoietic stem cell transplantation (HSCT) at the age of 8 years. One year after HSCT, his clinical condition had improved dramatically, suggesting that HSCT may be a long-term treatment option for young patients. Nevertheless, our results raise the possibility that selective p110δ inhibitors, such as GS-1101, may be an alternative effective therapeutic approach in APDS patients. GS-1101 (CAL-101 or Idelalisib) has been tested in phase 1 and 2 clinical trials for treatment of chronic lymphocytic leukemia ( The possibility of treating APDS patients with p110δ inhibitors should therefore be considered.

Supplementary Materials

Materials and Methods

Supplementary Text

Figs. S1 to S9

Tables S1 and S2

References (2737)

References and Notes

  1. Materials and methods are available as supplementary materials on Science Online.
  2. Acknowledgments: S.N. is a Wellcome Trust Senior Research Fellow in Basic Biomedical Science (095198/Z/10/Z). S.N. is also supported by the European Research Council (ERC) Starting grant 260477 and the European Union (EU) FP7 collaborative grant 261441 (PEVNET project). S.N., A.C., D.K., and R.D. are supported by the National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre. O.V. was supported by a Swiss National Science Foundation fellowship (grant PA00P3_134202) and a European Commission fellowship (FP7-PEOPLE-2010-IEF, no. 275880). R.L.W. was supported by the Medical Research Council (file reference U105184308). T.C. is supported by the National Children’s Research Centre, Our Lady’s Children’s Hospital, Crumlin, Dublin, Ireland. E.B.-H. is supported by a Wellcome Trust Translational Medicine and Therapeutics award. A.C. is supported by the Medical Research Council UK and the British Lung Foundation. K.O. is supported by a strategic grant from the Biotechnology and Biological Sciences Research Council and a New Investigator Award from the Wellcome Trust. P.H. and L.S. are funded by an Institute Programme grant from the Biotechnology and Biological Sciences Research Council (BB/J004456/1). S.K. is a Centre National de la Recherche Scientifique (CNRS) researcher. A.D., A.F., and S.K. are funded by Institut National de la Santé et de la Recherche Médicale; A.D. is supported by the EU FP7 EUROPAD contract 201549, Association Contre Le Cancer, and Agence Nationale de la Recherche (grant 2010-CSRD). A.F. is supported by the EU FP7 ERC PIDIMMUNE grant 249816. G.B.-M. was supported by a sabbatical grant from PASPA-DGAPA-UNAM. E.C. is a paid consultant for GlaxoSmithKline, Roche, and Novartis; A.C. is a paid consultant for GlaxoSmithKline; P.H. and L.S are paid consultants for GlaxoSmithKline and Karus Therapeutics Ltd; K.O. is a paid consultant for GlaxoSmithKline. Requests for DNA of individual patients will require informed consent from the patients and samples will be available under a material transfer agreement. The p110δ knockout mice are available from the Babraham Institute under a material transfer agreement. The mutation has been submitted to the ClinVar database; accession no. SCV000083058.

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