Kerttu Kalander
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Kerttu Kalander has a total of 28 co-authors. Here are the top co-authors by number of shared publications:
- Hector J. Monzo
Translational Cancer Medicine Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland
68 shared publications - Päivi M. Ojala
University of Helsinki
68 shared publications - Sirpa Leppä
University of Helsinki, Helsinki University Hospital Comprehensive Cancer Centre and iCAN Digital Precision Cancer Medicine Flagship, Helsinki, Finland
68 shared publications - Anna R. Makela
Department of Virology, University of Helsinki, Helsinki, Finland
34 shared publications - Kalle Saksela
Department of Virology, University of Helsinki, Helsinki, Finland
34 shared publications - Rogelio Antonio Hernández-López
Cell Design Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, USA
34 shared publications
Latest Publications
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 8 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S8. In vitro and in vivo activity of low a7inity scFv-guided CAR (KD = 3910 nM).
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 8 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S8. In vitro and in vivo activity of low a7inity scFv-guided CAR (KD = 3910 nM).
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 13 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S13. SKOV3 ovarian tumor volume measurements of individual mice treated with T cells expressing constitutive or inducible Sb1205 anti-HER2 CAR (related to Figure 5B and C).
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 13 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S13. SKOV3 ovarian tumor volume measurements of individual mice treated with T cells expressing constitutive or inducible Sb1205 anti-HER2 CAR (related to Figure 5B and C).
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 3 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S3. Antigen expression and HER2 knock-down in a panel of cancer cell lines and additional Jurkat T cell reporter activation (NFAT-GFP) assays in co-culture with 293T* (HER2 KD) cells transfected with tumor associated antigens (related to Figure 2C, 2D.
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 3 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S3. Antigen expression and HER2 knock-down in a panel of cancer cell lines and additional Jurkat T cell reporter activation (NFAT-GFP) assays in co-culture with 293T* (HER2 KD) cells transfected with tumor associated antigens (related to Figure 2C, 2D.
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 5 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S5. Cytotoxic activity of Sb CARs expressed in human primary CD8+ T cells (related to Figure 2E)
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 5 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S5. Cytotoxic activity of Sb CARs expressed in human primary CD8+ T cells (related to Figure 2E)
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 9 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S9. Tumor volume measurement of individual mice treated with T cells expressing Sb1205 anti-HER2 CAR (related to Figure 4C and E).
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 9 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S9. Tumor volume measurement of individual mice treated with T cells expressing Sb1205 anti-HER2 CAR (related to Figure 4C and E).
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Construct sequences from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Nucleotide sequences of constructs used in the study
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessConstruct sequences from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Nucleotide sequences of constructs used in the study
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 4 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S4. NFAT-EGFP reporter activation in Jurkat T cells exposed to phorbol myristateacetate (PMA) and ionomycin or co-cultured with target cells expressing the cognate tumor associated antigen.
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 4 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S4. NFAT-EGFP reporter activation in Jurkat T cells exposed to phorbol myristateacetate (PMA) and ionomycin or co-cultured with target cells expressing the cognate tumor associated antigen.
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 12 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S12. Statistical analysis of fraction of CD62L+CD45RA+ in T cells engineered with constitutive ScFv and SbCAR and inducible SbCAR (related to Figure 5A).
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 12 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S12. Statistical analysis of fraction of CD62L+CD45RA+ in T cells engineered with constitutive ScFv and SbCAR and inducible SbCAR (related to Figure 5A).
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 14 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S14. HCC1569 breast tumor volume measurements of individual mice treated with T cells expressing constitutive or inducible Sb1205 anti-HER2 CAR (related to Figure 5B).
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 14 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Figure S14. HCC1569 breast tumor volume measurements of individual mice treated with T cells expressing constitutive or inducible Sb1205 anti-HER2 CAR (related to Figure 5B).
- Open Access
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 1 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Supplementary Figure 1. Binding specificity of sherpabodies against a panel of promiscuouslyinteracting macromolecules
- 17 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 1 from Engineered SH3-Derived Sherpabodies Function as a Modular Platform for Targeted T-cell Immunotherapy
Supplementary Figure 1. Binding specificity of sherpabodies against a panel of promiscuouslyinteracting macromolecules