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Crystal L. Mackall, M.D.

Portait Photo of Crystal Mackall
Pediatric Oncology Branch
Head, Immunology Section
Branch Chief
Center for Cancer Research
National Cancer Institute
Building 10 - Hatfield CRC, Room 1W-3750
Bethesda, MD 20892-1104
Phone:  
301-402-5940
Fax:  
301-451-7010
E-Mail:  
cm35c@nih.gov

Biography

Crystal L. Mackall is Chief of the Pediatric Oncology Branch of the National Cancer Institute. She completed clinical training in Pediatrics and Internal Medicine, then came to the NCI in 1989 to undertake subspecialty training in Pediatric Hematology/Oncology. In 1990, Dr. Mackall initiated her scientific career under the mentorship of Ron Gress. During her postdoctoral work, she made pioneering discoveries regarding thymic function in humans and elucidated fundamental principles of T cell homeostasis. In 1998, she initiated an independent research program in the Immunology Section of the Pediatric Oncology Branch. Here, she has continued to make important contributions to our understanding of the biology of T cells homeostasis, she has led clinical development of interleukin-7 as a therapeutic immunorestorative and she has conducted translational studies of pediatric tumor immunology. She also leads a cutting edge clinical immunotherapy program that seeks to bring recent progress in tumor immunotherapy to the problem of childhood cancer. Dr. Mackall has received international recognition for her work on T cell homeostasis and tumor immunology. She is the recipient of numerous awards including the NIH Distinguished Clinical Teacher Award in 2000, an NCI Mentor of Merit Award in 2003, and several NCI Directors awards. She has authored over 130 scientific publications, is a member of the American Society of Clinical Investigation, and serves in numerous editorial and advisory positions. She is Board Certified in Internal Medicine, Pediatrics and Pediatric Hematology/Oncology.

Research

The mission of the Immunology Section of the Pediatric Oncology Branch is to develop effective immune based therapies for pediatric cancer.
Studies in the Mackall laboratory focus on three projects: 1) Biology and Therapy of Lymphopenia 2) Immunobiology and Immunotherapy of Pediatric Tumors and 3) Clinical Immunotherapy Program in Childhood Cancer. Specific aims of Project I are to improve understanding of the biology of T cell depletion in humans and to develop new approaches to enhance immune reconstitution or to exploit changes in physiology induced by lymphopenia. We previously elucidated an essential role for thymic pathways of T cell regeneration in the recovery from lymphopenia and described the limitations of this pathway present in cancer patients. We also discovered that interleukin-7, a cytokine produced by non-lymphoid stromal cells, augments thymic-independent immune reconstitution. In order to take these fundamental discoveries to the next level, we have devoted considerable effort to clinical development of rhIL7, as we hypothesized that treatment with this agent would overcome the limitations present in patients with cancer. We undertook the first-in-human trials of this agent, which demonstrated safety and biologic activity and we are currently conducting a trial of rhIL7, administered to children and young adults after treatment with dose intensive chemotherapy for high-risk pediatric solid tumors. Results thus far show the agent to be well tolerated, and potently able to hasten the pace of immune reconstitution following cytotoxic chemotherapy. Preliminary results also demonstrate that rhIL7 appears to augment responses to a tumor vaccine. More recent emerging studies have focused on increasing our understanding of soluble IL7R, which circulates in humans at high molar excess compared to IL-7, but has not been well studied. We were compelled to study this molecule because of recently published genetic data demonstrating that polymorphisms in IL7R predispose to autoimmunity. Our studies demonstrate that soluble IL7R is an important modulator of the bioactivity of IL-7 in vivo, such that increased levels substantially potentiate the activity IL-7, and therefore predispose to autoimmunity. Future studies will seek to determine whether soluble IL7R can be used to augment the potency of rhIL7 therapy.
Our second project focuses on identifying principles of tumor immunology as they relate to the embryonal tumors that occur in children and on inventing and developing new agents to target pediatric tumors. Much energy is currently focused on developing chimeric antigen receptors to target pediatric tumors, given the exciting preliminary data in clinical trials targeting tumors in adults with chimeric antigen receptors. Chimeric antigen receptors are likely to be highly effective at targeting pediatric tumors and their ability to target cell surface antigens, irrespective of HLA type, makes the clinical development of these agents for pediatric tumors a real possibility. We currently have active preclinical studies underway using several chimeric antigen receptors, including those targeting CD19, CD22, GD2, FGFR4, ALK and B7-H3. T cells expressing these receptors are generated in the laboratory, then tested in vitro for activity against cell lines and in xenograft models. Those with high level potency and a favorable predicted safety profile are prioritized for clinical development. We currently have one open clinical trial of CAR therapy targeting CD19+ acute lymphoblastic leukemia, and plan to open trials target GD2+ solid tumors and CD22+ acute lymphoblastic leukemia within the next 12 months.
Our third project is an active clinical trials program of immunotherapies in pediatric cancer. As discussed above, we are conducting the first in children trial of rhIL7 administered in the context of dendritic cell based tumor vaccines. We have also initiated a novel trial of activated NK cell therapy administered in patients with very high-risk solid tumors following allogeneic stem cell transplantation. This work builds on a previous study conducted by our group (Baird et al, Bio Blood and Marrow Transplant, 2011) wherein a non-myeloablative allogeneic peripheral blood stem cell transplant was administered to patients with ultra high-risk pediatric solid tumors. This study demonstrated a high level of safety and promising survival in this very high-risk population. In order to improve potency and to diminish the risk of GVHD, our current trial uses a T cell depletion platform following by administration of activated NK cells generated using 4-1BB expressing artificial antigen presenting cells plus IL15. This is highly novel and represents the first such use of 4-1BB/IL15 activated NK cells in humans. We also completed the first in children trial of anti-TRAIL receptor 2 therapies in pediatric solid tumors that was recently published in the Journal of Clinical Oncology (Merchant et al, J Clin Onc, 2012, In Press). Results demonstrate good tolerability, and some evidence for antitumor effects as well as intriguing data suggesting an interaction between irradiation and TRAIL-receptor 2 agonists. We are hopeful that this Phase I experience will provide the basis for future Phase II trials of TRAIL-Receptor 2 agonists in pediatric solid tumors. Finally, we are also conducting the first in children study of an immune checkpoint inhibitor, anti-CTLA4, which has demonstrated activity in adults with malignant melanoma.
In summary, we believe that there are many immunotherapies for childhood cancer that show promise for improving long term outcomes while avoiding the toxicity associated with traditional cytotoxic approaches. We posit that the recent dramatic progress in the field of immunotherapy for adult tumors can be leveraged to extend these therapies to pediatric cancer. Ultimately, we envision immunotherapy as a modality that can be added to future regimens that will employ less toxic doses of standard cytotoxic therapies to eradicate minimal residual disease and we envision that successful immunotherapy regimens are likely to be multimodal, including combinations of cell based therapies, monoclonal antibodies (or their derivatives), immunomodulators and/or cytokines.

This page was last updated on 10/28/2013.