Study of Mast Cell Precursors

The purpose of this protocol is to obtain large numbers of CD34+ cells from the peripheral
blood of healthy volunteers and patients with systemic mastocytosis or other related
allergic, hematological, and immunological conditions by leukapheresis for culture and
characterization of mast cell progenitor cells and their response to various cytokines and
anti-mitotic agents. Healthy volunteers and patients will be adults of both sexes from 18 to
70 years of age. Granulocyte colony stimulating factor (G-CSF) will be administered to
healthy volunteers at dose of 10 mcg/kg/day as a subcutaneous dose daily for 5 days not to
exceed 960mcg. Patients will receive Plerixafor at a dose of 0.24 mg/kg as a single
subcutaneous dose not to exceed 24mg the night before leukapheresis as a mobilizing agent for
CD34+ cells. In identified patients where leukapheresis yield is considered adequate without
stimulation by the principal investigator, leukapheresis may proceed without stimulation.
Healthy volunteers will undergo a single leukapheresis at day 7, and patients will undergo a
single leukapheresis at day 3 or 4. This is not a therapeutic protocol and does not involve
reinfusion of any manipulated cells, viruses or DNA constructs back into human subjects.

- SUBJECT INCLUSION CRITERIA:

Healthy Volunteers must:

1. Be 18-70 years of age

2. Be healthy

3. Have adequate peripheral venous access

4. Have normal renal function (creatinine less than or equal to 1.5mg/dL; less than or
equal to 1 plus proteinuria)

5. Have normal hepatic function (bilirubin less than or equal to 1.5 mg/dL)

6. Have normal hematologic function (WBC greater than or equal to 3000/mm(3);
granulocytes greater than or equal to 1500/mm(3) ; platelets greater than or equal to
175,000; hemoglobin greater than or equal to 12.5 g/dL)

Patients must:

1. Be 18-70 years of age

2. Have mast cell hyperplasia compatible with a diagnosis of systemic mastocytosis
(applicable to systemic mastocytosis patients only) or other allergic, hematologic, or
immunologic condition

3. Have adequate peripheral venous access or be willing to have a central line placed.

4. First be admitted as inpatients under an existing NIH protocol

5. Have preserved renal function (creatinine less than or equal to 2 mg/dL; less than or
equal to 2 plus proteinuria)

6. Have preserved hepatic function (bilirubin less than or equal to 1.5 mg/dL)

7. Have preserved hematologic function (WBC greater than or equal to 3000/mm(3);
granulocytes greater than or equal to 1500/mm(3) ; platelets greater than or equal to
175,000; hemoglobin greater than or equal to 12.5 g/dL)

All female subjects of childbearing potential:

1. May be enrolled if using effective contraception

2. Have a negative serum or urine pregnancy test determined within 72 hours before
beginning Plerixafor or G-CSF administration

SUBJECT EXCLUSION CRITERIA:

All subjects must not meet any of the following criteria:

Healthy volunteers and patients must not:

1. Have active bacterial, fungal or viral infections

2. Have viral screens positive for HIV or hepatitis B or C

3. Be pregnant or lactating

4. Have a history of autoimmune disease such as rheumatoid arthritis, vasculitis,
pyoderma gangrenosum or similar disorder

5. Have any condition, which in the judgment of the investigator, might place the subject
at undue risk

Healthy Volunteers with any of the following will be excluded:

1. Splenomegaly, pulmonary fibrosis and other related conditions

2. Use of any investigative drugs within the past 12 months

3. Have a significant coagulation disorder

Systemic Mastocytosis and Mast Cell Related Condition Patients with any of the following
will be excluded:

1. Patients taking any other growth factors, cytokines or investigative drugs

2. Patients who are hemodynamically unstable (blood pressure systolic of lower than 105
or diastolic lower than 65)