Reduced Intensity Conditioning for Hemophagocytic Syndromes or Selected Primary Immune Deficiencies (BMT CTN 1204)

Inclusion Criteria

• •1. Patient is ≥ 3 months and ≤ 45 years of age at time of enrollment.
• •2. Meets criteria for one of the following immune disorders (2A-2F) requiring HCT:
• •2A. HLH or related disorder with indication for HCT \[a. Inherited gene mutation associated with HLH: PRF1, UNC13D (MUNC13-2), STXBP2 (MUNC18-2), STX11, RAB27A (Griscelli syndrome, type 2), SH2D1A (XLP1), XIAP (XLP2), LYST (Chediak-Higashi syndrome) - OR - b. Meets clinical criteria for HLH, refractory to therapy according to HLH-94 or HLH-2004 (dexamethasone/etoposide), or recurrent episodes of hyper-inflammation - OR - c. Meets clinical criteria for HLH, without identified gene defects, with affected sibling - OR - decreased or absent NK cell function at the last evaluation, - OR - a history of CNS inflammation as evidenced by pleocytosis in CSF or MRI evidence of hyper-inflammation in the CNS\]
• •2B. CAEBV: Patients with chronic EBV infection (CAEBV) with or without associated lymphoma (in complete remission) or active HLH. Note that this diagnosis is distinct from post-transplant lymphoproliferative disorder/ EBV-associated lymphoproliferative disease (PTLD/LPD). \[Patients must meet all of the following: a. Severe progressive illness, usually with fever, lymphadenopathy and splenomegaly that either began as primary EBV infection or was associated with markedly elevated antibody titers to EBV viral capsid antibody (≥ 1:5120) or early antigen (≥ 1:640), or markedly elevated EBV DNA in the blood; - AND - b. Infiltration of tissues (e.g., lymph nodes, liver, lungs, CNS, bone marrow, eye, skin) with lymphocytes; - AND - c. Elevated EBV DNA, RNA or proteins in affected tissues; - AND - d. The absence of HIV or post-transplant lymphoproliferative disorder\]
• •2C. Chronic granulomatous disease with indication for HCT \[a. Oxidative burst \< 10% normal with dihydrorhodamine (DHR) assay - AND - b. Documented CGD mutation(s) in gp91phox, p47phox, p67phox, p22phox or p40phox - AND - c. Severe disease as evidenced by one or more of the following: history of one or more potentially life-threatening infections; inflammatory bowel disease; failure to thrive with height \<10% for age (unless parent(s) height \<10%); or autoimmune complication felt to be linked to CGD\]
• •2D. X-linked Hyper IgM Syndrome (HIGM1) \[a. Decreased serum IgG (more than 2 standard deviations below normal for age) - AND - b. Mutation in CD40LG - OR - family history of maternally related males with HIGM1\]
• •2E. IPEX Syndrome \[a. Absent FOXP3+ CD4+ T cells - OR - abnormal function of FOXP3+CD4+ T cells - AND - b. Disease-associated mutation in FoxP3 (bi-allelic in females) - OR - family history of maternally related males with clinical diagnosis of IPEX\]
• •2F. Severe Leukocyte Adhesion Deficiency, type I (LAD-I) \[a. Decreased CD18 expression on neutrophils (\<5% normal for age) - AND - b. Mutation of ITGB2 - OR - absence of ITGB2 mRNA in leukocytes\]
• •3\. Lansky or Karnofsky performance status ≥ 50%.
• •4\. The patient's donor must be willing and able to give bone marrow stem cells and be:
• •a. An unaffected sibling donor who is a 6/6 match at HLA-A and -B (intermediate or higher resolution) and -DRB1 (at high resolution using DNA-based typing) OR b. An unaffected related donor (other than sibling) who is a 7/8 or 8/8 match for HLA-A, -B, -C (at intermediate or higher resolution) and -DRB1 (at high resolution using DNA-based typing) OR c. An unrelated donor who is a 7/8 or 8/8 match at HLA-A, -B, -C, and -DRB1 (at high resolution using DNA-based typing).
• •5\. Patient must have adequate organ function as measured by:
• •1. Cardiac: Left ventricular ejection fraction (LVEF) \> 40%; or LV shortening fraction (LVSF) \> 26% by echocardiogram.
• •2. Renal: Calculated or radioisotope Glomerular Filtration Rate (GFR) \> 50 mL/min/1.73m\^2
• •3. Hepatic: Adequate liver function: serum conjugated (direct) bilirubin \< 2x upper limit of normal for age as per local laboratory (with the exceptions of isolated hyperbilirubinemia due to Gilbert's syndrome, or hyperbilirubinemia as the result of liver inflammation in the setting of persistent, active HLH); alanine aminotransferase (ALT) and aspartate aminotransferase (AST) \< 10x upper limit of normal as per local laboratory (with the exception of elevated transaminase levels as the result of liver inflammation in the setting of persistent, active HLH).
• •4. Pulmonary: Patient may not be on mechanical ventilation support or have progressive pulmonary infection at the time of transplant; Pulmonary Function Testing (PFT) with forced expiratory volume in one second (FEV1) \> 50% of normal and Diffusing capacity of the lung for carbon monoxide (DLCO) corrected for Hgb \> 50% of normal. Patients unable to undergo PFTs should have stable respiratory status with SaO2 \> 90% on a maximum of 2L/min supplemental oxygen.
• •6\. Signed informed consent.