T cells can be genetically modified to target tumors through the expression of a chimeric antigen receptor (CAR). Most notably, CAR T cells have demonstrated clinical efficacy in hematologic malignancies with more modest responses when targeting solid tumors. However, CAR T cells also have the capacity to elicit expected and unexpected toxicities including: cytokine release…
Molecular Therapy — Oncolytics Template
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About the Molecular Therapy — Oncolytics format
Molecular Therapy — Oncolytics is a peer-reviewed journal published by Elsevier, covering Virus-based gene therapy research, CAR-T cell therapy research, Immunotherapy and Immune Responses.
| Publisher | Elsevier |
|---|---|
| Reference style | Numbered (Elsevier) Numbered — [1], [2] in the text [1] A. Smith, B. Jones, C. Lee, A representative article title, Molecular Therapy — Oncolytics 12 (2023) 45–58.
Formats any DOI in Molecular Therapy — Oncolytics style. No sign-up. |
| Publishes research in | Virus-based gene therapy research CAR-T cell therapy research Immunotherapy and Immune Responses Cancer-related molecular mechanisms research MicroRNA in disease regulation |
| ISSN | 2372-7705 |
| h-index | 67 |
| i10-index | 669 |
| Total citations | 27,160 |
| Article processing charge | $3,200 |
| Open access | Yes |
| Top institutions publishing here | Sun Yat-sen University |
| Journal website | www.journals.elsevier.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
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Most-cited papers in Molecular Therapy — Oncolytics
The treatment of cancer patients with autologous T cells expressing a chimeric antigen receptor (CAR) is one of the most promising adoptive cellular therapy approaches. Reproducible manufacturing of high-quality, clinical-grade CAR-T cell products is a prerequisite for the wide application of this technology. Product quality needs to be built-in within every step of the manufacturing…
Oncolytic viruses (OVs) are powerful new therapeutic agents in cancer therapy. With the first OV (talimogene laherparepvec [T-vec]) obtaining US Food and Drug Administration approval, interest in OVs has been boosted greatly. Nevertheless, despite extensive research, oncolytic virotherapy has shown limited efficacy against solid tumors. Recent advances in viral retargeting, genetic editing, viral delivery platforms,…
Despite high remission rates following CAR-T cell therapy in B-ALL, relapse due to loss of the targeted antigen is increasingly recognized as a mechanism of immune escape. We hypothesized that simultaneous targeting of CD19 and CD22 may reduce the likelihood of antigen loss, thus improving sustained remission rates. A systematic approach to the generation of…
Chimeric antigen receptor (CAR) T cell therapy has demonstrated remarkable outcomes in individuals with hematological malignancies, but its success has been hindered by barriers intrinsic to the tumor microenvironment (TME), particularly for solid tumors, where it has yet to make its mark. In this article, we provide an updated review and future perspectives on features…