Single-Domain Antibodies for Targeting, Detection, and In Vivo Imaging of Human CD4+ Cells

被引:21
|
作者
Traenkle, Bjoern [1 ]
Kaiser, Philipp D. [1 ]
Pezzana, Stefania [2 ]
Richardson, Jennifer [3 ]
Gramlich, Marius [1 ]
Wagner, Teresa R. [1 ,4 ]
Seyfried, Dominik [2 ,5 ,6 ]
Weldle, Melissa [4 ]
Holz, Stefanie [4 ]
Parfyonova, Yana [4 ]
Nueske, Stefan [7 ]
Scholz, Armin M. [7 ]
Zeck, Anne [1 ]
Jakobi, Meike [1 ]
Schneiderhan-Marra, Nicole [1 ]
Schaller, Martin [8 ]
Maurer, Andreas [2 ]
Gouttefangeas, Cecile [3 ,5 ,6 ]
Kneilling, Manfred [2 ,8 ,9 ]
Pichler, Bernd J. [2 ,5 ,6 ,9 ]
Sonanini, Dominik [2 ,10 ]
Rothbauer, Ulrich [1 ,4 ,9 ]
机构
[1] Univ Tubingen, NMI Nat & Med Sci Inst, Reutlingen, Germany
[2] Univ Tubingen, Dept Preclin Imaging & Radiopharm, Werner Siemens Imaging Ctr, Tubingen, Germany
[3] Univ Tubingen, Inst Cell Biol, Dept Immunol, Tubingen, Germany
[4] Univ Tubingen, Pharmaceut Biotechnol, Tubingen, Germany
[5] German Canc Consortium DKTK, Tubingen, Germany
[6] German Canc Res Ctr DKFZ Partner Site Tubingen, Tubingen, Germany
[7] Ludwig Maximilians Univ Munchen, Livestock Ctr, Fac Vet Med, Oberschleissheim, Germany
[8] Univ Tubingen, Dept Dermatol, Tubingen, Germany
[9] Univ Tubingen, Cluster Excellence iFIT EXC2180 Image Guided & Fu, Tubingen, Germany
[10] Univ Tubingen, Dept Med Oncol & Pneumol, Tubingen, Germany
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
关键词
CD4; nanobody; immune tracer; PET imaging; magnetic resonance imaging; immunotherapies; EXCHANGE MASS-SPECTROMETRY; T-CELLS; MONOCLONAL-ANTIBODY; RHEUMATOID-ARTHRITIS; NANOBODY; ANTI-CD4; EXPRESSION; LYMPHOCYTES; BINDING; GROWTH;
D O I
10.3389/fimmu.2021.799910
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The advancement of new immunotherapies necessitates appropriate probes to monitor the presence and distribution of distinct immune cell populations. Considering the key role of CD4(+) cells in regulating immunological processes, we generated novel single-domain antibodies [nanobodies (Nbs)] that specifically recognize human CD4. After in-depth analysis of their binding properties, recognized epitopes, and effects on T-cell proliferation, activation, and cytokine release, we selected CD4-specific Nbs that did not interfere with crucial T-cell processes in vitro and converted them into immune tracers for noninvasive molecular imaging. By optical imaging, we demonstrated the ability of a high-affinity CD4-Nb to specifically visualize CD4(+) cells in vivo using a xenograft model. Furthermore, quantitative high-resolution immune positron emission tomography (immunoPET)/MR of a human CD4 knock-in mouse model showed rapid accumulation of Cu-64-radiolabeled CD4-Nb1 in CD4(+) T cell-rich tissues. We propose that the CD4-Nbs presented here could serve as versatile probes for stratifying patients and monitoring individual immune responses during personalized immunotherapy in both cancer and inflammatory diseases.
引用
收藏
页数:17
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