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Review Article

Disease modeling of immunological disorders using induced pluripotent stem cells

Pages 68-74 | Received 11 May 2018, Accepted 23 May 2018, Published online: 07 Sep 2018

Figures & data

Figure 1. A principle for directed differentiation of human PSCs to hematopoietic cells. Human PSCs can be differentiated into hematopoietic progenitor cells by a defined monolayer condition. Hematopoietic progenitor cells are then committed to each hematopoietic lineage by optimizing the cytokine setting.

Figure 1. A principle for directed differentiation of human PSCs to hematopoietic cells. Human PSCs can be differentiated into hematopoietic progenitor cells by a defined monolayer condition. Hematopoietic progenitor cells are then committed to each hematopoietic lineage by optimizing the cytokine setting.

Figure 2. Immortalization of hematopoietic progenitor cells from human PSCs. Hematopoietic progenitor cells can be immortalized by introducing appropriate transcription factors.

Figure 2. Immortalization of hematopoietic progenitor cells from human PSCs. Hematopoietic progenitor cells can be immortalized by introducing appropriate transcription factors.

Figure 3. Identification of somatic NLRC4 mutation from a patient with autoinflammation. The patient’s genetic background was identified through iPSC-based phenotype analysis.

Figure 3. Identification of somatic NLRC4 mutation from a patient with autoinflammation. The patient’s genetic background was identified through iPSC-based phenotype analysis.

Figure 4. Establishment of a PSC-based disease model for Blau syndrome. Establishment of genome-edited isogenic counterparts enables precise phenotypic comparisons to study disease-associated mutations.

Figure 4. Establishment of a PSC-based disease model for Blau syndrome. Establishment of genome-edited isogenic counterparts enables precise phenotypic comparisons to study disease-associated mutations.