Measurement of T cell alloreactivity using imaging flow cytometry
The measurement of immunological reactivity to donor antigens in transplant recipients is likely to be crucial for the successful reduction or withdrawal of immunosuppression. The mixed leukocyte reaction (MLR), limiting dilution assays, and trans-vivo delayed-type hypersensitivity (DTH) assay have...
| Main Authors: | , , , , , |
|---|---|
| Format: | Journal article |
| Language: | English |
| Published: |
Journal of Visualised Experiments
2017
|
| _version_ | 1797098932620230656 |
|---|---|
| author | Juvet, S Moshkelgosha, S Sanderson, S Hester, J Wood, K Bushell, A |
| author_facet | Juvet, S Moshkelgosha, S Sanderson, S Hester, J Wood, K Bushell, A |
| author_sort | Juvet, S |
| collection | OXFORD |
| description | The measurement of immunological reactivity to donor antigens in transplant recipients is likely to be crucial for the successful reduction or withdrawal of immunosuppression. The mixed leukocyte reaction (MLR), limiting dilution assays, and trans-vivo delayed-type hypersensitivity (DTH) assay have all been applied to this question, but these methods have limited predictive ability and/or significant practical limitations that reduce their usefulness. Imaging flow cytometry is a technique that combines the multiparametric quantitative powers of flow cytometry with the imaging capabilities of fluorescent microscopy. We recently made use of an imaging flow cytometry approach to define the proportion of recipient T cells capable of forming mature immune synapses with donor antigen-presenting cells (APCs). Using a well-characterized mouse heart transplant model, we have shown that the frequency of in vitro immune synapses among T-APC membrane contact events strongly predicted allograft outcome in rejection, tolerance, and a situation where transplant survival depends on induced regulatory T cells. The frequency of T-APC contacts increased with T cells from mice during acute rejection and decreased with T cells from mice rendered unresponsive to alloantigen. The addition of regulatory T cells to the in vitro system reduced prolonged T-APC contacts. Critically, this effect was also seen with human polyclonally expanded, naturally occurring regulatory T cells, which are known to control the rejection of human tissues in humanized mouse models. Further development of this approach may allow for a deeper characterization of the alloreactive T-cell compartment in transplant recipients. In the future, further development and evaluation of this method using human cells may form the basis for assays used to select patients for immunosuppression minimization, and it can be used to measure the impact of tolerogenic therapies in the clinic. |
| first_indexed | 2024-03-07T05:16:37Z |
| format | Journal article |
| id | oxford-uuid:dd70bbc4-8f02-4e9c-991e-d57e174d0c8e |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T05:16:37Z |
| publishDate | 2017 |
| publisher | Journal of Visualised Experiments |
| record_format | dspace |
| spelling | oxford-uuid:dd70bbc4-8f02-4e9c-991e-d57e174d0c8e2022-03-27T09:25:01ZMeasurement of T cell alloreactivity using imaging flow cytometryJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:dd70bbc4-8f02-4e9c-991e-d57e174d0c8eEnglishSymplectic Elements at OxfordJournal of Visualised Experiments2017Juvet, SMoshkelgosha, SSanderson, SHester, JWood, KBushell, AThe measurement of immunological reactivity to donor antigens in transplant recipients is likely to be crucial for the successful reduction or withdrawal of immunosuppression. The mixed leukocyte reaction (MLR), limiting dilution assays, and trans-vivo delayed-type hypersensitivity (DTH) assay have all been applied to this question, but these methods have limited predictive ability and/or significant practical limitations that reduce their usefulness. Imaging flow cytometry is a technique that combines the multiparametric quantitative powers of flow cytometry with the imaging capabilities of fluorescent microscopy. We recently made use of an imaging flow cytometry approach to define the proportion of recipient T cells capable of forming mature immune synapses with donor antigen-presenting cells (APCs). Using a well-characterized mouse heart transplant model, we have shown that the frequency of in vitro immune synapses among T-APC membrane contact events strongly predicted allograft outcome in rejection, tolerance, and a situation where transplant survival depends on induced regulatory T cells. The frequency of T-APC contacts increased with T cells from mice during acute rejection and decreased with T cells from mice rendered unresponsive to alloantigen. The addition of regulatory T cells to the in vitro system reduced prolonged T-APC contacts. Critically, this effect was also seen with human polyclonally expanded, naturally occurring regulatory T cells, which are known to control the rejection of human tissues in humanized mouse models. Further development of this approach may allow for a deeper characterization of the alloreactive T-cell compartment in transplant recipients. In the future, further development and evaluation of this method using human cells may form the basis for assays used to select patients for immunosuppression minimization, and it can be used to measure the impact of tolerogenic therapies in the clinic. |
| spellingShingle | Juvet, S Moshkelgosha, S Sanderson, S Hester, J Wood, K Bushell, A Measurement of T cell alloreactivity using imaging flow cytometry |
| title | Measurement of T cell alloreactivity using imaging flow cytometry |
| title_full | Measurement of T cell alloreactivity using imaging flow cytometry |
| title_fullStr | Measurement of T cell alloreactivity using imaging flow cytometry |
| title_full_unstemmed | Measurement of T cell alloreactivity using imaging flow cytometry |
| title_short | Measurement of T cell alloreactivity using imaging flow cytometry |
| title_sort | measurement of t cell alloreactivity using imaging flow cytometry |
| work_keys_str_mv | AT juvets measurementoftcellalloreactivityusingimagingflowcytometry AT moshkelgoshas measurementoftcellalloreactivityusingimagingflowcytometry AT sandersons measurementoftcellalloreactivityusingimagingflowcytometry AT hesterj measurementoftcellalloreactivityusingimagingflowcytometry AT woodk measurementoftcellalloreactivityusingimagingflowcytometry AT bushella measurementoftcellalloreactivityusingimagingflowcytometry |