| 000 | 02084nam a2200361 4500 | ||
|---|---|---|---|
| 001 | ESSALUD | ||
| 005 | 20260820161112.0 | ||
| 007 | ta | ||
| 008 | t pe ||||| |||| 00| 0 spa d | ||
| 040 | _aBMG | ||
| 041 | _aeng | ||
| 100 |
_aBhoj, Vijay G. _eAutor _954193 |
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| 245 | _aKidney transplantation in two highly sensitized candidates after CAR T-Cell therapy | ||
| 300 | _apáginas: 2117-2125 | ||
| 520 | _aHLA sensitization poses a major challenge to kidney transplantation for patients with end-stage kidney disease, especially for highly sensitized candidates. Attempts at antibody elimination (desensitization) have had inconsistent efficacy and have often failed to produce sustained reductions in anti-HLA antibodies in patients with the highest level of sensitization (calculated panel-reactive antibody score, ≥99.9%). We now report the results for the safety run-in cohort of a multicenter phase 1 clinical study evaluating the safety and efficacy of combined CD19-targeted and B-cell maturation antigen (BCMA)–targeted chimeric antigen receptor (CAR) T cells in eliminating the cellular sources of preformed anti-HLA antibodies (ClinicalTrials.gov number, NCT06056102). Kidney transplantation was performed in two highly sensitized candidates after desensitization with the use of dual CAR T-cell therapy. | ||
| 650 |
_aENFERMEDAD RENAL CRÓNICA _932213 |
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| 650 |
_aTRASPLANTE DE RIÑÓN _913898 |
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| 650 |
_aCIRUGÍA GENERAL _944496 |
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| 650 |
_aCÉLULAS T _954097 |
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| 650 |
_aTRASPLANTE _97847 |
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| 700 |
_aKaminski, María _954194 |
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| 700 |
_aZhao, Huiwu _954195 |
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| 700 |
_aJackson, Kyle _954196 |
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| 700 |
_aWang, Wei _954197 |
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| 700 |
_aLiu, Chengyang _954198 |
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| 700 |
_aMontgomery, Robert A. _954199 |
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| 700 |
_aAli, Nicole _954200 |
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| 700 |
_aMangiola, Massimo _954201 |
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| 700 |
_aSpitzer, Thomas R. _954202 |
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| 700 |
_aSafa, Kassem _954203 |
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| 773 | 0 |
_022717 _922648 _dMassachusetts NEJM Group _oNEJM011 _tThe New England Journal of Medicine _wESSALUD _x0028-4793 |
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| 942 |
_cARTICULOS _e2026-08-20 _zsqb |
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| 999 |
_c22842 _d22842 |
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