The Jackson Laboratory

NSG® Variants Portfolio

NSG (NOD scid gamma) mice are the foundational platform for developing humanized models capable of replicating a myriad of in vivo immune cell and tumor combinatorial environments. As such, these are the models of choice for a range of research areas, with thousands of publications in support of immuno-oncology, autoimmunity, metabolics, neurobiology, cardiovascular and infectious disease studies.

Optimize your study design when you select models which carry transgenic expression of critical cytokines, targeted gene knockouts, or combinations of both:

  • Cytokine expression - models express critical cytokines that support development and long-term stability of immune cell types
  • Knockout of Major Histocompatibility Complex (MHC) Types I & II to significantly decrease the development of GvHD upon human cell or tumor engraftment
  • Advanced immunodeficient strains for HSC engraftment, where targeted gene mutations (e.g. c-Kit receptor) enable cell engraftment without irradiation

NSG models are available in a variety of ways to order, from off-the-shelf options to highly-customizable options and combinations of cell-and tumor-engraftment. Models can be shipped to your research institute or may be enrolled directly into a JAX Preclinical Services Study.

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The Jackson Laboratory - NSG® Variants Portfolio - Immune System Components

Comparison of NSG Mouse Model Variants

Strain NamesModel BenefitsStrain ConsiderationsReference

NSG*
(005557)

  • Successful xenografts of human tumors and primary cells
  • T cell-dependent inflammatory responses
  • Optimal human hematopoietic stem cell engraftment (Sirpa allele)
  • No scid-associated leakiness
  • No thymic lymphoma (long lifespan >22 months)
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

Stokol et al., 2026
Gudenas et al., 2026
Chong et al., 2026

NSG-SGM3
(013062)

  • Enhanced human myelopoiesis and terminal differentiation on HSC engraftment
  • Increased efficiency of engrafting human acute myeloid leukemia (AML)
  • Increased CD4+ FoxP3+ regulatory T cells on HSC engraftment
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development
  • Macrophage Activated Syndrome
  • Compromised human stem cell regeneration
  • Suppression of human erythropoiesis
  • Reduction of human B-lymphopoiesis

Thibodeau et al., 2026
Tandaric et al., 2026
Khanal et al., 2025

NSG-FLT3
(033367)
CD34 Humanized Data

  • Improved development of dendritic cells (cDCs and pDCs), monocytes, NK cells and mucosal immune system, upon HSC engraftment
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

Yang et al., 2026
Dreaden et al., 2025

NSG-SGM3-IL15
(033216)
CD34 Humanized Data

  • Expression of human IL15 enhances the development of human NK cells. This strain may be useful for studying immunotherapies targeting NK cells and NK cell function in tumorigenesis.
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development
  • Macrophage activated Syndrome

Dreaden et al., 2025

New

NSG-FLT3-IL15
(037322)
CD34 Humanized Data

  • Enhanced reconstitution of T cells, Tregs, myeloid cells, and mature natural killer cells
  • High expression of conventional and plasmacytoid dendritic cells
  • Diversity of immune cell models enables evaluation of combinatorial therapies that target T cells, NK cells, and relevant tumor microenvironment cells
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development
 

NSG-MHC I/II DKO
(025216)

  • Mouse MHC knockouts provide delayed GvHD response, with study durations up to 90 days post PBMC engraftment
  • T cell-dependent inflammatory responses
  • Extended human IgG half-life compared to B2m knockouts
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

Snook et al., 2026
Tsai et al., 2026
Liu et al., 2025
Moore et al., 2025

New

NSG-SGM3-IL15-DKO
(037320)
PBMC Humanized Data

  • Expression of a complex immune cell profile, including myeloid, NK, T cell and mature B cell populations
  • Ideal for evaluation of therapies such as T cell engagers or in vivo CAR T studies in a more complex human immune cell environment
  • Major Histocompatibility Complex (MHC) I/II gene knockouts delay GvHD, enabling an experimental study window of 75-100 days
  • Repeatable studies with Reserved Pre-Characterized PBMCs from JAX
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • No de novo IgG secretion
 

NBSGW
(026622)

  • Human CD34 cells engraft effectively without preconditioning irradiation
  • Longer lifespan than other immunodeficient Kit mutants
  • Increased human erythroid cells (bone marrow)
  • Although irradiation is not required for stem cell engraftment, NBSGW mice likely share the same sensitivity to genotoxic agents as other NSG strains

Chhan et al., 2026
Mejia-Ramirez et al., 2026
Park et al., 2025
Nikeghbal et al., 2025

NRG
(007799)

  • Long-term multilineage hematopoeitic stem cell repopulation similar to NSG mice
  • T cell-dependent inflammatory responses
  • Engrafts human PBMC without irradiation similar to NSG
  • Engrafts a wide range of solid and hematological cancers
  • Greater tolerance to genotoxic agents compared to NSG
  • Resistant to irradiation
  • Resistant to genotoxic drugs
  • Optimal human hematopoietic stem cell engraftment (Sirpa allele)
  • No scid-associated leakiness
  • Longer life span than NOD scid (> 22 months)
  • Requires higher dose of irradiation to obtain human HSC engraftment
  • The serum half-life of human IgG is greatly reduced in NSG-B2m due to defective FcRn function
  • Immature B Cell development

Kunika et al., 2025
Alshiraihi et al., 2025
Kumari et al., 2023

NSG-A2
(009617)

  • High engraftment of HLA-A2-restricted immune cells after CD34+ humanization
  • Antibody responses improved in a Dengue virus infection model
  • Allow HLA restriction of developing human CD8 cells in humanized models, and provide improved platforms for viral infection and vaccine models
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

Xue et al., 2024
Kalinina et al., 2024

NSG-HLA-A2/HHD
(014570)

  • Enable functional CD4+ T cell responses to viral infection after CD34+ humanization
  • Permit HLA restriction and enhance immune responses of human CD8 T cells
  • Antibody responses improved in a Dengue virus infection model
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

O'Brien et al., 2025
Boardman et al., 2025
Wardell et al., 2025

NSG-DR1
(012479)

  • Useful for transplantation studies in the absence of xeno-GVHD
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development
  • Reduced CD45+ cell engraftment compared to NSG

Serreze et al., 2025

NSG-Abo DR4
(017637)

  • Useful for transplantation studies in the absence of xeno-GVHD
  • Develop allo-GVHD post-engraftment of DR4-negative CD4+ T cells
  • Show enhanced antibody responses, and human CD4+ T cells interact more effectively with human antigen presenting cells
  • Reduced CD45+ cell engraftment compared to NSG
  • Higher proportion of mice with no CD45+ cell engraftment as compared to NSG

Serreze et al., 2025
Aron et al., 2022

NSG B2m
(010636)

  • Resistant to xeno-GVHD
  • Useful for studying mechanisms for xeno-GVHD
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

Kumari et al., 2023
Apriamashvili et al., 2022

NSG-(KbDb)null
(023848)

  • Attenuated xeno-GVHD development post-Hu-PBMC transplantation
  • High Hu-CD45+ cell engraftment
  • Useful for studying mechanisms for xeno-GVHD
  • Reduced survival post Hu-CD34+ cell transplantation compared to NSG mice

Shultz et al., 2019

NSG-PiZ
(028842)

  • Engrafts human and allogeneic mouse hepatocytes without rejection
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

Monian et al., 2026
Smith et al., 2024
Lu et al., 2024

NSG-TLR4 KO
(033704)

  • Residual mouse innate immune system cannot respond to Tlr4 agonists
  • After humanization, NSG-Tlr4 KO are ideal for studying human TLR4-specific responses against tumors
  • scid side effects: radiation sensitivity; genotoxic drugs may have higher toxicity
  • Immature B Cell development

Aryee et al., 2023

*NSG® is a registered trademark in the USA and other countries.

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