Alpha/Beta T and CD19+ Depleted Peripheral Stem Cells for Patients With Primary Immunodeficiencies

This is a Phase II trial to determine the ability of a reduced intensity conditioning regimen
to allow successful engraftment with alpha/beta T and CD19+ depleted peripheral stem cell
grafts from unrelated or partially matched related donors. There are two conditioning
regimens depending upon patient diagnosis and age.

The study will include patients 0-22 years with PID, including immune dysregulation syndromes
for which hematopoietic stem cell transplant is indicated.

Treatment: Either conditioning regimen (listed below) followed by alpha/beta T and CD19+
depleted donor peripheral stem cells

1. Reduced intensity conditioning with busulfan x 8 doses, fludarabine 40 mg/m2 x 4,
thiotepa 5 mg/kg x 2, ATG 3 mg/kg x 3.

OR

2. Myeloablative regimen with busulfan x 16 doses or Daily for four days, fludarabine 30
mg/m2 x 5, thiotepa 5 mg/kg x 2, ATG 3 mg/kg x 2.

OR

3. Immunotherapy regimen on days -9, 8, 7 with anti-thymocyte globulin 3 mg/kg/day (for
severe combined immunodeficiency patients only).

4. Infusion of alpha/beta T and CD19+ depleted donor peripheral stem cells.

5. Follow up, including evaluation of chimerism and immune reconstitution.

Inclusion Criteria:

1. Ages 0-22 years at time of enrollment

2. Diseases:

- Immunodeficiencies for which allogeneic hematopoietic stem cell transplant is
indicated, including severe combined immunodeficiencies, IPEX syndrome, X-linked
lymphoproliferative disease, chronic granulomatous disease, WAS, hyperIgM, and
other life-threatening immunodeficiencies.

- Immune dysregulation syndromes, including refractory or recurrent hemophagocytic
lymphohistiocytosis, HLH with genetic mutations, refractory multisystemic
Langerhans cell histiocytosis, other MAS refractory to standard therapy.

3. Clinical status

- Lansky or Karnofsky performance >=60

- Organ Function:

1. Serum creatinine <1.5 x upper limit of normal for age Hepatic: ALT <=250;
AST <=350

2. Cardiac shortening fraction >=27%

3. Bilirubin <2.5x normal (unless elevation due to Gilberts disease).

4. No active untreated infection

4. Signed informed consent

5. No HLA matched related donor available.

6. Females of childbearing potential must have negative pregnancy test.

Exclusion Criteria:

- Uncontrolled bacterial, viral or fungal infections

- HLA matched related or unrelated donor able to donate mobilized peripheral stem cells.

- Pregnant Females

- Matched related donor available for bone marrow donation

Donors Selection Criteria:

- Donor selection will comply with 21 CFR 1271

- Unrelated donor matched or up to one antigen mismatch as per National Marrow Donor
Program (NMDP).

- Haploidentical parent or sibling able to undergo mobilization for peripheral stem cell
collection. Maternal donor preferred over paternal donor if both equally
haploidentical.

- CHOP BMT procedures apply for determining donor eligibility, including donor screening
and testing for relevant communicable disease agents and diseases.

- Unrelated donor identified through the National Marrow Donor Program (NMDP) and
fulfills the NMDP criteria for donation. Unrelated donor willing and able to undergo
mobilization of peripheral stem cells and apheresis