Mechanistic Elucidation and Therapeutic Improvement of Anti-CTLA-4 Therapies
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lax-blax-phd-cheme-2023-thesis.pdf
Description
Thesis PDF
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6.02 MB
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Adobe PDF
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1e368e173ca3a31f83ee37f74b1891f1
Author(s)
Lax, Brianna Marie
Advisor(s)
Wittrup, K. Dane
Date Issued
June 2023
Publisher
Massachusetts Institute of Technology
Abstract
Anti-CTLA-4 antibodies have successfully elicited durable tumor regression in the clinic; however, long-term benefit is limited to a subset of patients for select cancer indications. The incomplete understanding of their mechanism of action has hindered efforts at improvement, with conflicting hypotheses proposing either antagonism of the CTLA-4:B7 axis or Fc effector-mediated regulatory T cell (Treg) depletion governing efficacy. Here we report the engineering of a non-antagonistic CTLA-4 binding domain (b1s1e2) that depletes intratumoral Tregs as an Fc fusion. Comparison of b1s1e2-Fc to 9d9, an antagonistic anti-CTLA-4 antibody, allowed for determination of the separate contributions of CTLA-4 antagonism and Treg depletion to efficacy. Despite equivalent levels of intratumoral Treg depletion, 9d9 achieved more long-term cures than b1s1e2-Fc in MC38 tumors, demonstrating that CTLA-4 antagonism provided additional survival benefit. Consistent with prior reports that CTLA-4 antagonism enhances priming, treatment with 9d9, but not b1s1e2-Fc, increased the percentage of activated T cells in the tumor-draining lymph node (tdLN). Treg depletion with both constructs was restricted to the tumor due to insufficient surface CTLA-4 expression on Tregs in other compartments to elicit Fc effector-mediated Treg depletion. Through intratumoral administration of diphtheria toxin (DT) in Foxp3-DTR mice, we show that depletion of both intratumoral and intranodal Tregs provided even greater survival benefit than 9d9, consistent with Treg-mediated restraint of priming in the tdLN. Lastly, we engineered a CTLA-4-targeted enzyme fusion as a potentially translatable approach for combined intratumoral and intranodal Treg depletion. Preliminary data suggest that CTLA-4 targeting increases local Treg death as a result of proximal enzymatic activity, but further characterization remains to be done. Overall, our data demonstrate that anti-CTLA-4 therapies require both CTLA-4 antagonism and intratumoral Treg depletion for maximum efficacy - but that future therapies capable of depleting intranodal Tregs could show superior efficacy, even in the absence of CTLA-4 antagonism.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
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