JITC Digest April 2026

By JITC Publications posted 4 hours ago

  

INSIDE THIS ISSUE:  

Letter from the Editor| JITC  Editor Picks|JITC Meet-the-Editor Session at AAI|Popular Archive Articles

Letter from the Editor

Hello JITC Readers, 

As the spring opens up with a series of meetings arising, including the recent WIC-APAC (World Immunotherapy Council Asia-Pacific in Taiwan), the annual AAI (American Association of Immunology in Boston April 15-19), where I will be holding meet-the-editor sessions on both Thursday, April 16, and Friday, April 17, at the SITC booth (see the special feature below for more details), this year’s AACR (American Association of Cancer Research in San Diego April 17-22), the IUIS (International Union of Immunology Societies) Day of Immunology on April 29, the TIMO (Tumor Immunology Meets Oncology in Brandenburg May 7-9), and CIMT (the Association for Cancer Immunotherapy in Mainz May 11-13), the surfeit of meetings and multiple letter meetings will keep the IO (Immuno-Oncology!) field brewing with new findings and evidence that spring has indeed arrived! On that note, I have been excited to see new findings on ‘T’ cells and the activity of the thymus reported with evidence of so-called thymic health being critical for response to ICB (immune checkpoint blockade) by Simon Bernatz, et al.

In the early ’60s, Jacques Miller demonstrated that T cells, which require the thymus and are named “T cells,” in contrast to Bruce Glick’s demonstration of B cells arising from the Bursa of Fabricius in birds, were a separate and defined lineage of lymphocytes. Now we have several means to measure ‘thymic health,’ including CT measures of the thymus size and density within the superior mediastinum, so-called T cell receptor excision circles (TRECs) in the blood using RT-PCR, and full T and B cell repertoire analysis (the adaptome) in the periphery and within the tumor (diversity and clonality, respectively). Integrating these studies into modern understanding of aging, cancer, and response to therapy represent exciting opportunities for the field.

 

Oncolytic and Local Immunotherapy Section
One of our newest sections in JITC focuses on how local therapies can change systemic biology, perhaps mediated in part by emergence and recruitment of new T cells arising from the thymus. It is headed up by Section Editor, Howard Kaufman, MD, FACS at Harvard and Ankyra Therapeutics. He is joined by Associate Editors Praveen Bommareddy, PhD at Replimune Inc.; Darrel J. Irvine, PhD at Scripps Research in LaJolla; Balveen Kaur, PhD at LSU LCMC Health Cancer Center; Liang-Tzung Lin, PhD at Taipei Medical UniversitySamuel Rabkin, PhD at Massachusetts General Hospital; K. Dane Wittrup, PhD at Massachusetts Institute of Technologyand Dmitriy Zamarin, MD, PhD at Icahn School of Medicine at Mount Sinai.

Recently Howard and colleagues (Joshua Brody, MD from Icahn School of Medicine at Mount SinaiTanja de Gruijl, PhD at Amsterdam University Medical Centers; and Aurélien Marabelle, MD, PhD at Gustave Roussy) ran a virtual summit with SITC on Intralesional Therapy. We are now preparing a special series headed up by this group. The first manuscript of the series and some of the original research we will share with you for this month’s digest.

Highlighted Manuscripts 

I would like to emphasize the importance of oncolytic and local therapies as part of our mission for the Journal. Here we focus on “what the study adds” messaging from the articles themselves, selected from those published recently. I encourage you to peruse them and the other papers published in JITC this last month.

Regards, 

Michael T. Lotze, MD, FAIO
Editor-in-Chief
Journal for ImmunoTherapy of Cancer

JITC Editor Picks

Effects of oncolytic immunotherapy with RP1 (vusolimogene oderparepvec) on immune cells mediate responsiveness to anti-PD-1 via STING-mediated interferon signaling

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From the Authors – What This Study Adds:
  • This study demonstrates distinct responses to usolimogene oderparepvec (RP1) between tumor and immune cells, and how tumor cells coordinate responses to the signals generated by immune cells. Our findings provide a mechanistic insight into how RP1 reshapes the tumor microenvironment and highlight the importance of STING in activating RP1-induced interferon responses in immune cells, which drive PD-L1 expression.

Priorities for local immunotherapy research and drug development  

From the Authors:
  • A “Summit on Intralesional Immunotherapy” was held in September 2024, which comprised lectures and discussion from an international panel of experts on local immune therapy. In this consensus paper, we discuss unique considerations for local immunotherapy development across the continuum from pre-clinical and early-stage investigation through registration intent clinical trials.

Liver-directed AAV-IL-10 therapy enhances CD8+ T cell-mediated immunity against hepatocellular carcinoma

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From the Authors:
  • We demonstrate that liver-directed delivery of IL-10 using an adeno-associated virus vector not only reduces tumor burden but also reshapes the liver immune landscape by enhancing CD8+ T-cell effector function and promoting the development of long-lived, tissue-resident memory-like CD8T cells.

Dual-chemokine-armed oncolytic Senecavirus A co-recruits cDC1 and CXCR3+ T cells to convert ‘cold’ melanoma and drive durable regression

From the Authors – What This Study Adds:

  • This study provides direct evidence that coordinated intratumoral delivery of CXCL11 and vXCL1 via an oncolytic Senecavirus A (SVA) virus induces synergistic antitumor immunity, an effect unattainable by single-chemokine therapies. We further demonstrate that signal peptide deletion did not compromise the therapeutic outcome, as evidenced by well-preserved antitumor efficacy and a comparable overall survival benefit. Crucially, our results reveal that this combination therapy drives comprehensive remodeling of the immune-cold tumor microenvironment by enhancing dendritic cell activation, CD8T cell infiltration, and M1 macrophage polarization, which collectively leads to deep and durable tumor regression.

Meet-the-Editor Sessions at AAI

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For those attending the 2026 American Association of Immunology (AAI) annual meeting, visit the SITC booth #1031 in the exhibit hall and meet JITC Editor-in-Chief Dr. Michael T. Lotze during two JITC Meet-the-Editor Sessions:

  • Thursday, April 16, 11:30am– 12:30pm
  • Friday, April 17, 11:30am– 12:30pm

Stop by to say hello to Dr. Lotze, share your research, and learn more about JITC. For additional information during AAI 2026, check out JITC’s  and  profiles

Popular Archive Articles 

The selections below represent some of the most popular content published in JITC over the past two years. Explore additional thematic content in JITC 's Collections or access the rest of JITC 's archives for a look at all the journal has to offer.

An oncolytic vaccinia virus encoding hyaluronidase reshapes the extracellular matrix to enhance cancer chemotherapy and immunotherapy (7 March 2024) 
RESEARCH

Oncolytic herpes simplex virus expressing IL-2 controls glioblastoma growth and improves survival (9 April 2024) 
RESEARCH

Phase I dose-escalation and pharmacodynamic study of STING agonist E7766 in advanced solid tumors  (20 February 2025) 
RESEARCH

Oncolytic virus OH2 extends survival in patients with PD-1 pretreated melanoma: phase Ia/Ib trial results and biomarker insights  (6 February 2025) 
RESEARCH 

Don’t Forget to Check Out These Other Great  JITC Special Series:
Cancer Immunotherapy in Understudied Populations (2024-2025)
The Next Wave of Immuno-Oncology: A Roadmap from SITC (2024-2025) 
Computational Immuno-Oncology  (2023-2025) 


APC Discounts

As a way to thank the SITC members who work tirelessly to advance the science and improve the lives of cancer patients, SITC members who are first, last, or corresponding authors on JITC articles at the time of acceptance will receive discounted Article Processing Charges (APCs) . This discount is applied post-acceptance, at which point a discount code is shared with the corresponding author. Learn more .

JITC also offers full waivers for the full APC (100% discount of the APC) where all authors are based in low-income countries (see policy). Requests for waivers must be made prior to submission. For additional information regarding these discounts, as well as institutional arrangements and editor/reviewer discounts, view the journal's APC policy . Additional questions may be directed to JITC Editor@sitcancer.org.

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