Mapping Therapeutic Regulatory T Cell Fate with MRI: Current Strategies and Translational Outlook.

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Title: Mapping Therapeutic Regulatory T Cell Fate with MRI: Current Strategies and Translational Outlook.
Authors: Ping, Yu1 (AUTHOR), Chen, Lydia1,2 (AUTHOR), Hoenig, Jacob Joel1 (AUTHOR), Yang, Xiaohan1,2 (AUTHOR), Chapelin, Fanny1,2 (AUTHOR) fachapelin@ucsd.edu
Source: Nanomaterials (2079-4991). Jun2026, Vol. 16 Issue 11, p691. 24p.
Subjects: Regulatory T cells, Intracellular tracking, Graft versus host disease, Immunologic diseases, Graft rejection, Autoimmune diseases
Abstract: Adoptive cell therapies, and more specifically, regulatory T cell (Treg) therapies, have shown significant therapeutic promise across multiple immune-mediated diseases including graft-versus-host disease (GvHD), solid organ transplant (SOT) rejection, and autoimmune diseases. One key challenge is the lack of insight into the biodistribution and fate of adoptively transferred T cells and Tregs in living organisms. These uncertainties delay progress on establishing optimal dosage(s), infusion timing and route, as well as investigations into off-target effects. Magnetic resonance imaging (MRI) cell tracking is particularly beneficial in this setting because it enables real-time, deep-tissue coverage without ionizing radiation. In this review, we compare existing MRI T cell tracking strategies using iron oxide particles and fluorinated agents. We describe preclinical and clinical applications of MRI for cell therapy tracking and provide a perspective on the potential impact on the field. [ABSTRACT FROM AUTHOR]
Copyright of Nanomaterials (2079-4991) is the property of MDPI and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Mapping Therapeutic Regulatory T Cell Fate with MRI: Current Strategies and Translational Outlook.
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  Data: <searchLink fieldCode="AR" term="%22Ping%2C+Yu%22">Ping, Yu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Lydia%22">Chen, Lydia</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hoenig%2C+Jacob+Joel%22">Hoenig, Jacob Joel</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yang%2C+Xiaohan%22">Yang, Xiaohan</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chapelin%2C+Fanny%22">Chapelin, Fanny</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> fachapelin@ucsd.edu</i>
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  Data: <searchLink fieldCode="JN" term="%22Nanomaterials+%282079-4991%29%22">Nanomaterials (2079-4991)</searchLink>. Jun2026, Vol. 16 Issue 11, p691. 24p.
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  Data: <searchLink fieldCode="DE" term="%22Regulatory+T+cells%22">Regulatory T cells</searchLink><br /><searchLink fieldCode="DE" term="%22Intracellular+tracking%22">Intracellular tracking</searchLink><br /><searchLink fieldCode="DE" term="%22Graft+versus+host+disease%22">Graft versus host disease</searchLink><br /><searchLink fieldCode="DE" term="%22Immunologic+diseases%22">Immunologic diseases</searchLink><br /><searchLink fieldCode="DE" term="%22Graft+rejection%22">Graft rejection</searchLink><br /><searchLink fieldCode="DE" term="%22Autoimmune+diseases%22">Autoimmune diseases</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Adoptive cell therapies, and more specifically, regulatory T cell (Treg) therapies, have shown significant therapeutic promise across multiple immune-mediated diseases including graft-versus-host disease (GvHD), solid organ transplant (SOT) rejection, and autoimmune diseases. One key challenge is the lack of insight into the biodistribution and fate of adoptively transferred T cells and Tregs in living organisms. These uncertainties delay progress on establishing optimal dosage(s), infusion timing and route, as well as investigations into off-target effects. Magnetic resonance imaging (MRI) cell tracking is particularly beneficial in this setting because it enables real-time, deep-tissue coverage without ionizing radiation. In this review, we compare existing MRI T cell tracking strategies using iron oxide particles and fluorinated agents. We describe preclinical and clinical applications of MRI for cell therapy tracking and provide a perspective on the potential impact on the field. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Nanomaterials (2079-4991) is the property of MDPI and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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      – Type: doi
        Value: 10.3390/nano16110691
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      – Code: eng
        Text: English
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        PageCount: 24
        StartPage: 691
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      – SubjectFull: Regulatory T cells
        Type: general
      – SubjectFull: Intracellular tracking
        Type: general
      – SubjectFull: Graft versus host disease
        Type: general
      – SubjectFull: Immunologic diseases
        Type: general
      – SubjectFull: Graft rejection
        Type: general
      – SubjectFull: Autoimmune diseases
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      – TitleFull: Mapping Therapeutic Regulatory T Cell Fate with MRI: Current Strategies and Translational Outlook.
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            NameFull: Ping, Yu
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            NameFull: Chen, Lydia
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            NameFull: Hoenig, Jacob Joel
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            NameFull: Yang, Xiaohan
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              M: 06
              Text: Jun2026
              Type: published
              Y: 2026
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