1. Applying dosing schedules to the clinical protocols of combinatorial
therapy, we can optimize the clinical outcome 4-14-2010
In 1986, a clinical protocol for the treatment of advanced malignant melanoma with
the newly discovered class of immune cells called TIL was initiated at the National
Institutes of Health (NIH). These lymphocytes are T cells that are isolated directly from
the tumor and that are then grown to large numbers in tissue culture in the presence of the
T cell growth factor interleukin-2 (IL2). After expansion in culture several thousand
times, approximately 2 X 10" TIL are given to the patient intravenously in addition to
high doses of IL-2 in several days of treatment. Even in those patients who did not
respond to all other therapy (including treatment with IL-2 alone), 35 to 40% of patients
responded to this protocol.
The large-scale tissue culture and the large numbers of cells and IL-2 that are given to a
patient make this procedure expensive and clinically difficult. Furthermore, 60 to 65% of
patients fail to respond to this treatment, and even those who do respond will often fail
after 6 to 12 months. It is likely that only a subset of the heterologous population of cells
administered to a patient are effective in killing cancer cells in vivo.
That was then (1986) and this is now 2009. Dr. Rosenberg and colleagues have optimized
the protocol to generate a response rate of 72% using lymphodepletion prior to Adaptive
Cell Therapy.
It cannot be certain that the TIL subsets preferentially recovered from the tumor biopsy
corresponded to those that mediated complete elimination of tumor in this patient.
Recently, a patient that went down to NIH and did the ACT therapy had a response only where
the cells came from (lungs). The other tumors continued to progress.
Are the TILs tumor specific based on where the cells were obtained during biopsy? Does this
mean the other tumors mutated or are they missing some receptor or MHC I or II at the tumor
surface?
The property of the T-CELL RECEPTOR which enables it to react with some
antigens and not others. The specificity is derived from the structure of the
receptor's variable region which has the ability to recognize certain antigens in
conjunction with the MAJOR HISTOCOMPATIBILITY COMPLEX molecule.
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2. Adoptive Cell Transfer.. 57 days after transfer. CD8+ T-cell (CTLs) at the Maximum
Propagation
A tumor lesion excised from patient 9 before nonmyeloablating chemotherapy
("pretreatment") exhibited scant CD8+ cells (left), strong stromal cell staining but weak
staining of tumor cells with antibody to MHC class I (center), and sporadic cell staining
with an antibody to MHC class II (probably tumor macrophages) but minimal staining of
tumor cells (right). In contrast, a sample resected 57 days after cell transfer ("post
treatment") exhibited a dense, diffuse CD8+ infiltrate and ubiquitous expression of both
MHC class I and class II molecules in tumor cells.
Source: Cancer Regression and Autoimmunity in Patients After Clonal
Repopulation with Antitumor Lymphocytes
Originally published in Science Express on 19 September 2002
Science 25 October 2002:
Vol. 298. no. 5594, pp. 850 - 854
DOI: 10.1126/science.1076514
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3. Patients undergoing Anti-CTLA-4 Blockadge. Week7 = Day 49 maximum ALC.. CD8+
T-cell (CTLs)
Source: Dr. Jedd Wolchok
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4. What I am trying to show is the growth curves for the various T-cells subsets with data
from in vivo to back up the above graphic. With that in mind, we now have a better
understanding on the growth patterns of these cells. By applying dosing schedules to the
clinical protocols of combinatorial therapy, we can optimize the clinical outcome.
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