The TCR δ Repertoire in Normal Human Skin is Restricted and Distinct from the TCR δ Repertoire in the Peripheral Blood

Sequences of proteins of immunological interest

Kabat, B. E. A. (1984) · Analytical Biochemistry · doi:10.1016/0003-2697(84)90805-4 · Cited by 3,363

Simplified mammalian DNA isolation procedure

Laird, P. W., Zijderveld, A., Linders, K., Rudnicki, M. A., Jaenisch, R., & Berns, A. J. M. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.15.4293 · Cited by 1,497

Recognition of Stress-Induced MHC Molecules by Intestinal Epithelial γδ T Cells

Groh, V., Steinle, A., Bauer, S., & Spies, T. A. (1998) · Science · doi:10.1126/science.279.5357.1737 · Cited by 1,142

γδ Cells: A Right Time and a Right Place for a Conserved Third Way of Protection

Hayday, A. (2000) · Annual Review of Immunology · doi:10.1146/annurev.immunol.18.1.975 · Cited by 1,134

Broad tumor-associated expression and recognition by tumor-derived γδ T cells of MICA and MICB

Groh, V., Rhinehart, R. L., Secrist, H., Bauer, S., Grabstein, K. H., & Spies, T. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.12.6879 · Cited by 1,026

Lymphocytes bearing antigen-specific γδ T-cell receptors accumulate in human infectious disease lesions

Modlin, R. L., Pirmez, C., Hofman, F. M., Torigian, V. K., Uyemura, K., Rea, T. H., Bloom, B. R., & Brenner, M. B. (1989) · Nature · doi:10.1038/339544a0 · Cited by 573

Limited diversity of γδ antigen receptor genes of thy-1+ dendritic epidermal cells

Asarnow, D. M., Kuziel, W. A., Bonyhad, M., Tigelaar, R. E., Tucker, P. W., & Allison, J. P. (1988) · Cell · doi:10.1016/0092-8674(88)90139-0 · Cited by 517

CDR3 length in antigen-specific immune receptors.

Rock, E. P., Sibbald, P. R., Davis, M. M., & Chien, Y. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.1.323 · Cited by 515

The anatomical basis of intestinal immunity

Mowat, A. M., & Viney, J. L. (1997) · Immunological Reviews · doi:10.1111/j.1600-065x.1997.tb00966.x · Cited by 493

Inflammatory Skin Diseases, T Cells, and Immune Surveillance

Robert, C., & Kupper, T. S. (1999) · New England Journal of Medicine · doi:10.1056/nejm199912093412407 · Cited by 474

Imiquimod-Induced Psoriasis-Like Skin Inflammation in Mice Is Mediated via the IL-23/IL-17 Axis

van der Fits, L., Mourits, S., Voerman, J. S. A., Kant, M., Boon, L., Laman, J. D., Cornelissen, F., Mus, A.-M. C., Florencia, E. F., Prens, E. P., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802999 · Cited by 2,259

Regulation of Cutaneous Malignancy by γδ T Cells

Girardi, M., Oppenheim, D. E., Steele, C. R., Lewis, J. M., Glusac, E. J., Filler, R. B., Hobby, P., Sutton, B. J., Tigelaar, R. E., & Hayday, A. (2001) · Science · doi:10.1126/science.1063916 · Cited by 1,068

Does the Immune System See Tumors as Foreign or Self?

Pardoll, D. M. (2003) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141135 · Cited by 770

Intraepithelial lymphocytes: exploring the Third Way in immunology

Hayday, A., Theodoridis, E., Ramsburg, E., & Shires, J. (2001) · Nature Immunology · doi:10.1038/ni1101-997 · Cited by 491

γδ T cells in homeostasis and host defence of epithelial barrier tissues

Nielsen, M. M., Witherden, D. A., & Havran, W. L. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.101 · Cited by 479

The emerging roles of γδ T cells in cancer immunotherapy

Mensurado, S., Blanco-Domínguez, R., & Silva‐Santos, B. (2023) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-022-00722-1 · Cited by 359

Identification of a Novel Proinflammatory Human Skin-Homing Vγ9Vδ2 T Cell Subset with a Potential Role in Psoriasis

Laggner, U., Meglio, P. D., Perera, G. K., Hundhausen, C., Lacy, K. E., Ali, N., Smith, C. H., Hayday, A., Nickoloff, B. J., & Nestle, F. O. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100804 · Cited by 324

γδ T Cells Link Innate and Adaptive Immune Responses

Holtmeier, W., & Kabelitz, D. (2005) · KARGER eBooks · doi:10.1159/000086659 · Cited by 305

Skint1, the prototype of a newly identified immunoglobulin superfamily gene cluster, positively selects epidermal γδ T cells

Boyden, L. M., Lewis, J. M., Barbee, S. D., Bas, A., Girardi, M., Hayday, A., Tigelaar, R. E., & Lifton, R. P. (2008) · Nature Genetics · doi:10.1038/ng.108 · Cited by 299

Immunosurveillance and Immunoregulation by γδ T Cells

Girardi, M. (2005) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700003 · Cited by 286

Cutaneous immunosurveillance by self-renewing dermal γδ T cells

Sumaria, N., Roediger, B., Ng, L. G., Qin, J., Pinto, R., Cavanagh, L. L., Shklovskaya, E., Groth, B. F. D. S., Triccas, J. A., & Weninger, W. (2011) · The Journal of Experimental Medicine · doi:10.1084/jem.20101824 · Cited by 286

Homing and Function of Human Skin γδ T Cells and NK Cells: Relevance for Tumor Surveillance

Ebert, L. M., Meuter, S., & Moser, B. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.7.4331 · Cited by 243

Resident Skin-specific γδ T Cells Provide Local, Nonredundant Regulation of Cutaneous Inflammation

Girardi, M., Lewis, J. M., Glusac, E. J., Filler, R. B., Geng, L., Hayday, A., & Tigelaar, R. E. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20012000 · Cited by 195

The Distinct Contributions of Murine T Cell Receptor (TCR)γδ+ and TCRαβ+ T Cells to Different Stages of Chemically Induced Skin Cancer

Girardi, M., Glusac, E. J., Filler, R. B., Roberts, S. J., Propperova, I., Lewis, J. M., Tigelaar, R. E., & Hayday, A. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20021282 · Cited by 182

Tissue-resident immune cells in humans

Gray, J. I., & Farber, D. L. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-093019-112809 · Cited by 181

Innate immune functions of human γδ T cells

Beetz, S., Wesch, D., Marischen, L., Welte, S., Oberg, H., & Kabelitz, D. (2007) · Immunobiology · doi:10.1016/j.imbio.2007.10.006 · Cited by 144

Plasticity of γδ T Cells: Impact on the Anti-Tumor Response

Lafont, V., Sanchez, F., Laprévotte, E., Michaud, H., Gros, L., Eliaou, J.-F., & Bonnefoy, N. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00622 · Cited by 154

Tissue Adaptations of Memory and Tissue-Resident Gamma Delta T Cells

Khairallah, C. F., Chu, T. H., & Sheridan, B. S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02636 · Cited by 140

γδ T Lymphocytes: An Effector Cell in Autoimmunity and Infection

Shiromizu, C. M., & Jancic, C. C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02389 · Cited by 135

γδ T cells: firefighters or fire boosters in the front lines of inflammatory responses

Nanno, M., Shiohara, T., Yamamoto, H., Kawakami, K., & Ishikawa, H. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2006.00474.x · Cited by 109

Toll‐Like Receptor Expression and Function in Subsets of Human γδ T Lymphocytes

Pietschmann, K., Beetz, S., Welte, S., Martens, I., Gruen, J., Oberg, H., Wesch, D., & Kabelitz, D. (2009) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2009.02290.x · Cited by 94

Innate and adaptive γδ T cells: How, when, and why

Papadopoulou, M., Sanchez, G. S., & Vermijlen, D. (2020) · Immunological Reviews · doi:10.1111/imr.12926 · Cited by 99

Gamma Delta T Cells and Their Pathogenic Role in Psoriasis

Qi, C., Wang, Y., Li, P., & Zhao, J. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.627139 · Cited by 93

Effect Of Human Natural Killer and γδ T Cells on the Growth of Human Autologous Melanoma Xenografts in SCID Mice

Lozupone, F., Pende, D., BURGIO, V. L., Castelli, C., Spada, M., Venditti, M., Luciani, F., Lugini, L., Federici, C., Ramoni, C., et al. (2004) · Cancer Research · doi:10.1158/0008-5472.can-03-1501 · Cited by 90

Comparing Mouse and Human Tissue-Resident γδ T Cells

Qu, G., Wang, S., Zhou, Z., Jiang, D., Liao, A., & Luo, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.891687 · Cited by 87

New Insights Into the Regulation of γδ T Cells by BTN3A and Other BTN/BTNL in Tumor Immunity

Blazquez, J.-L., Benyamine, A., Pasero, C., & Olive, D. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01601 · Cited by 88

Tissue-resident immune cells: from defining characteristics to roles in diseases

Li, J., Chu, X., Li, C., & He, J. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02050-5 · Cited by 87

Defects in Skin γδ T Cell Function Contribute to Delayed Wound Repair in Rapamycin-Treated Mice

Mills, R. E., Taylor, K. R., Podshivalova, K., McKay, D. B., & Jameson, J. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.6.3974 · Cited by 79

Development of the neonatal B and T cell repertoire in swine: implications for comparative and veterinary immunology

Butler, J. E., Šinkora, M., Wertz, N., Holtmeier, W., & Lemke-Miltner, C. D. (2006) · Veterinary Research · doi:10.1051/vetres:2006009 · Cited by 78

T-cell receptor repertoire in pyoderma gangrenosum: evidence for clonal expansions and trafficking

Brooklyn, T., Williams, A. M., Dunnill, M. G. S., & Probert, C. S. (2007) · British Journal of Dermatology · doi:10.1111/j.1365-2133.2007.08211.x · Cited by 77

Regulation of skin cell homeostasis by gamma delta T cells

Julie, M. J. (2004) · Frontiers in bioscience · doi:10.2741/1423 · Cited by 79

CD4+ T cells producing interleukin (IL)‐17, IL‐22 and interferon‐γ are major effector T cells in nickel allergy

Dyring‐Andersen, B., Skov, L., Løvendorf, M. B., Bzorek, M., Søndergaard, K., Lauritsen, J.-P. H., Dabelsteen, S., Geisler, C., & Bonefeld, C. M. (2013) · Contact Dermatitis · doi:10.1111/cod.12043 · Cited by 74

Dissecting the complexity of γδ T-cell subsets in skin homeostasis, inflammation, and malignancy

Castillo‐González, R., Cibrián, D., & Sánchez‐Madrid, F. (2020) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2020.11.023 · Cited by 72

Human Vδ2 versus non-Vδ2 γδ T cells in antitumor immunity

Kabelitz, D., Kalyan, S., Oberg, H., & Wesch, D. (2013) · OncoImmunology · doi:10.4161/onci.23304 · Cited by 67

PD-1 defines a distinct, functional, tissue-adapted state in Vδ1+ T cells with implications for cancer immunotherapy

Davies, D., Kamdar, S., Woolf, R., Zlatareva, I., Iannitto, M. L., Morton, C., Haque, Y., Martin, H., Biswas, D., Ndagire, S., et al. (2024) · Nature Cancer · doi:10.1038/s43018-023-00690-0 · Cited by 67

Regulatory functions of γδ T cells

Kabelitz, D., Peters, C., Wesch, D., & Oberg, H. (2013) · International Immunopharmacology · doi:10.1016/j.intimp.2013.01.022 · Cited by 60

Stress, NK Receptors, and Immune Surveillance

Pardoll, D. M. (2001) · Science · doi:10.1126/science.1066284 · Cited by 58

Environmentally Responsive and Reversible Regulation of Epidermal Barrier Function by γδ T Cells

Girardi, M., Lewis, J. M., Filler, R. B., Hayday, A., & Tigelaar, R. E. (2006) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700120 · Cited by 57

All hands on DE(T)C: Epithelial-resident γδ T cells respond to tissue injury

Ramirez, K., Witherden, D. A., & Havran, W. L. (2015) · Cellular Immunology · doi:10.1016/j.cellimm.2015.04.003 · Cited by 57

The Multifunctionality of Human Vγ9Vδ2 γδ T Cells: Clonal Plasticity or Distinct Subsets?

Kabelitz, D., & He, W. (2012) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2012.02727.x · Cited by 54

Innate Lymphocytes in Psoriasis

Polese, B., Zhang, H., Thurairajah, B., & King, I. L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00242 · Cited by 54

T-cell effector mechanisms: γδ and CD1d-restricted subsets

Jameson, J., Witherden, D. A., & Havran, W. L. (2003) · Current Opinion in Immunology · doi:10.1016/s0952-7915(03)00045-1 · Cited by 53

Dendritic Cells and T Cells in the Regulation of Cutaneous Immunity

Loser, K., & Beissert, S. (2007) · Advances in Dermatology · doi:10.1016/j.yadr.2007.07.014 · Cited by 52

Skin immune surveillance by T cells—A new order?

Strid, J., Tigelaar, R. E., & Hayday, A. (2009) · Seminars in Immunology · doi:10.1016/j.smim.2009.03.002 · Cited by 52

γδ T Cells in Cancer Immunotherapy: Current Status and Future Prospects

Chiplunkar, S. V., Dhar, S., Wesch, D., & Kabelitz, D. (2009) · Immunotherapy · doi:10.2217/imt.09.27 · Cited by 49

Gamma/Delta T Cells and Their Role in Protection Against Malaria

Deroost, K., & Langhorne, J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02973 · Cited by 47

The Role of Tissue-resident γδ T Cells in Stress Surveillance and Tissue Maintenance

Johnson, M. D., Witherden, D. A., & Havran, W. L. (2020) · Cells · doi:10.3390/cells9030686 · Cited by 46

Development and Compartmentalization of the Porcine TCR δ Repertoire at Mucosal and Extraintestinal Sites: The Pig as a Model for Analyzing the Effects of Age and Microbial Factors

Holtmeier, W., Kaeller, J., Geisel, W., Pabst, R., Caspary, W. F., & Rothkötter, H. J. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.4.1993 · Cited by 43

Current Perspectives on the Use of off the Shelf CAR-T/NK Cells for the Treatment of Cancer

Cutmore, L. C., & Marshall, J. F. (2021) · Cancers · doi:10.3390/cancers13081926 · Cited by 35

The Role of theγδT Cell in Allergic Diseases

Zheng, R., & Yang, Q. (2014) · Journal of Immunology Research · doi:10.1155/2014/963484 · Cited by 30

Gamma delta T cells and their immunotherapeutic potential in cancer

Cieslak, S. G., & Shahbazi, R. (2025) · Biomarker Research · doi:10.1186/s40364-025-00762-6 · Cited by 33

Cutaneous T cell immunity

Zareie, P., Weiss, E. S., Kaplan, D. H., & Mackay, L. K. (2025) · Nature Immunology · doi:10.1038/s41590-025-02145-3 · Cited by 29

Local γδ T cells: translating promise to practice in cancer immunotherapy

Zlatareva, I., & Wu, Y. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02303-0 · Cited by 25

T cell receptor δ repertoire in inflamed and noninflamed colon of patients with IBD analyzed by CDR3 spectratyping

Holtmeier, W., Hennemann, A., May, E., Duchmann, R., & Caspary, W. F. (2002) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00224.2001 · Cited by 24

A Long-Playing CD about the γδ TCR Repertoire

Hayday, A., & Vantourout, P. (2013) · Immunity · doi:10.1016/j.immuni.2013.11.016 · Cited by 22

Immunosurveillance by γδ T Cells: Focus on the Murine System

Girardi, M., & Hayday, A. (2005) · KARGER eBooks · doi:10.1159/000086658 · Cited by 21

Dendritic Epidermal T Cells in Allergic Contact Dermatitis

Mraz, V., Geisler, C., & Bonefeld, C. M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00874 · Cited by 22

Identification of a novel lymphoid population in the murine epidermis

Almeida, F. F., Tenno, M., Brzostek, J., Li, J. L. Y., Allies, G., Hoeffel, G., See, P., Ng, L. G., Fehling, H. J., Gascoigne, N. R. J., et al. (2015) · Scientific Reports · doi:10.1038/srep12554 · Cited by 19

γδ T Cell and Other Immune Cells Crosstalk in Cellular Immunity

He, Y. Z., Wu, K., Hu, Y., Sheng, L., Tie, R., Wang, B., & Huang, H. (2014) · Journal of Immunology Research · doi:10.1155/2014/960252 · Cited by 21

Dermal-Resident versus Recruited γδ T Cell Response to Cutaneous Vaccinia Virus Infection

Davis, A. S. W., Bergsbaken, T., Delaney, M. A., & Bevan, M. J. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402438 · Cited by 20

Assessment of Immune Response Following Dendritic Cell-Based Immunotherapy in Pediatric Patients With Relapsing Sarcoma

Fědorová, L., Múdry, P., Pilátová, K., Selingerová, I., Merhautová, J., Řehák, Z., Valík, D., Hlaváčková, E. O., Cerna, D., Faberova, L., et al. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01169 · Cited by 18

Innate Lymphocyte Mechanisms in Skin Diseases

Chen, Y., Hardman, C. S., Yadava, K., & Ogg, G. S. (2020) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082919-093554 · Cited by 18

TCR usage in naive and committed alloreactive cells: implications for the understanding of TCR biases in transplantation

Guillet, M., Sébille, F., & Soulillou, J. (2001) · Current Opinion in Immunology · doi:10.1016/s0952-7915(00)00260-0 · Cited by 18

Human γδ T cells: From a neglected lymphocyte population to cellular immunotherapy: A personal reflection of 30years of γδ T cell research

Kabelitz, D. (2016) · Clinical Immunology · doi:10.1016/j.clim.2016.07.012 · Cited by 17

Distinct TCR δ repertoires are present in the cutaneous lesions and inflamed duodenum of patients with dermatitis herpetiformis

Holtmeier, W., Pfänder, M., Zollner, T. M., Kaufmann, R., & Caspary, W. F. (2002) · Experimental Dermatology · doi:10.1034/j.1600-0625.2002.110605.x · Cited by 16

Gamma delta T cells in cancer therapy: from tumor recognition to novel treatments

Luo, X., Lv, Y., Yang, J., Long, R., Qiu, J.-Y., Deng, Y., Tang, G., Zhang, C., Li, J., & Zuo, J. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1480191 · Cited by 16

Natural Self-Ligand Gamma Delta T Cell Receptors (γδTCRs) Insight: The Potential of Induced IgG

de Sousa, T. R., & Victor, J. R. (2020) · Vaccines · doi:10.3390/vaccines8030436 · Cited by 14

Conventional and Unconventional T Cells

Roberts, S. J., & Girardi, M. (2008) · Springer eBooks · doi:10.1007/978-1-84800-165-7_6 · Cited by 18

Calcitonin gene-related peptide upregulates IL-17A and IL-22 in γδ-T cells through the paracrine effect of langerhans cells on LC/γδ-T co-culture model

Peng, F., Zhao, S., Zhang, X., Long, S., & He, Y. (2021) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2021.577792 · Cited by 13

Get in Touch With Dendritic Epithelial T Cells!

Thelen, F., & Witherden, D. A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01656 · Cited by 14

Gamma/delta intraepithelial lymphocytes in the mouse small intestine

Ogata, M., & Itoh, T. (2016) · Anatomical Science International · doi:10.1007/s12565-016-0341-2 · Cited by 12

Characterization of γδ T cells in naïve and HIV ‐infected chimpanzees and their responses to T ‐cell activators in vitro

Hodara, V. L., Parodi, L. M., Chavez, D., Smith, L. M., Lanford, R. E., & Giavedoni, L. D. (2014) · Journal of Medical Primatology · doi:10.1111/jmp.12115 · Cited by 6

Spectratype analysis of the T cell receptor δ CDR3 region of bovine γδ T cells responding to leptospira

Herzig, C. T. A., Mailloux, V. L., & Baldwin, C. L. (2014) · Immunogenetics · doi:10.1007/s00251-014-0817-y · Cited by 6

Lower incidence of grade II-IV acute Graft-versus-Host-Disease in pediatric patients recovering with high Vδ2+ T cells after allogeneic stem cell transplantation with unmanipulated bone marrow grafts: a prospective single-center cohort study

Müller, T., Alasfar, L., Preuß, F., Zimmermann, L., Streitz, M., Hundsdörfer, P., Eggert, A., Schulte, J. H., von Stackelberg, A., & Oevermann, L. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1433785 · Cited by 4

Graft-versus-host disease is associated with skewed γδ T-cell clonality after umbilical cord blood transplantation in children with nonmalignant diseases

Winstead, M., Hill, M. J., Amin, Z., Lugt, M. T. V., Chen, X., & Szabolcs, P. (2023) · Cytotherapy · doi:10.1016/j.jcyt.2023.06.003 · Cited by 4

Fundamentals of Feto-Neonatal Immunology and Its Clinical Relevance

Maheshwari, A., & LaGamma, E. L. (2012) · Springer eBooks · doi:10.1007/978-88-470-1405-3_108 · Cited by 4

Tick Extracellular Vesicles Alter Epidermal Keratinocyte Function

Marnin, L., Valencia, L. M., Bogale, H. N., Laukaitis-Yousey, H. J., Rolandelli, A., Ferraz, C. R., O’Neal, A. J., Schmitter-Sánchez, A. D., Bencosme-Cuevas, E., Nguyen, T.-T., et al. (2025) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2025.08.037 · Cited by 4

Vδ2neg γ δ T Cells, a Multi-Reactive Tissue Subset: from Innate to Adaptive Altered-Self Surveillance

Behr, C., Capone, M., Couzi, L., Taupin, J., & Déchanet‐Merville, J. (2014) · The Open Immunology Journal · doi:10.2174/1874226200902010106 · Cited by 4

Roles of dendritic epidermal T cells in steady and different pathological states

Hao, J., Zhang, J., & Liu, Y. (2024) · Burns & Trauma · doi:10.1093/burnst/tkae056 · Cited by 3

Structure of the Skin and Cutaneous Immunology

Plager, D. A., Bieber, T. R. M., & Pittelkow, M. R. (2014) · Elsevier eBooks · doi:10.1016/b978-0-323-08593-9.00034-6 · Cited by 4

Neonatal Immunity

Maheshwari, A., Khuder, S., Lawrence, S. M., & Christensen, R. D. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-69415-5.00056-4 · Cited by 3

Distribution and development of the postnatal murine Vδ1 T‐cell receptor repertoire

Holtmeier, W., Gille, J., Zeuzem, S., & Šinkora, M. (2010) · Immunology · doi:10.1111/j.1365-2567.2010.03290.x · Cited by 3

Role of γδ T Lymphocytes in the Pathogenesis of Autoimmune Diseases with Skin Lesions

Sorokina, E. V., Bisheva, I. V., Mishina, N. V., & Stolpnikova, V. N. (2023) · Успехи современной биологии · doi:10.31857/s0042132423010088 · Cited by 2

Complex Interplays in Immune T-Cell Differentiation and Developmental Fate Determination

Duc, H. T. (2011) · Immunotherapy · doi:10.2217/imt.11.95 · Cited by 2

Skin: Immunological Defence Mechanisms

Shiu, J., Harberts, E. M., Gaspari, A. A., & Nickoloff, B. J. (2013) · Wiley eBooks · doi:10.1002/9780470015902.a0001215.pub3 · Cited by 2

Gamma-Delta T Cells in the Skin

Tan, S., Tay, S. S., Sumaria, N., Roediger, B., & Weninger, W. (2017) · Springer eBooks · doi:10.1007/978-3-319-29785-9_4 · Cited by 2

Fundamentals of Feto-Neonatal Immunology

Maheshwari, A., & Gamma, E. F. L. (2018) · Springer eBooks · doi:10.1007/978-3-319-29489-6_246 · Cited by 1

Neonatal Leukocyte Physiology and Disorders

Benjamin, J. T., Torres, B. A., & Maheshwari, A. (2018) · Avery's Diseases of the Newborn · doi:10.1016/b978-0-323-40139-5.00083-8 · Cited by 1

Unconventional T Cells

Hayday, A., & Steele, C. R. (2010) · Wiley eBooks · doi:10.1002/9780470688618.taw0104

The role of γδ T cells in human cutaneous oncology

Alaibac, M., Pigozzi, B., & Bordignon, M. (2006) · Expert Review of Dermatology · doi:10.1586/17469872.1.2.293

Structural and Functional Cutaneous Immunology

Plager, D. A., & Pittelkow, M. R. (2009) · Elsevier eBooks · doi:10.1016/b978-0-323-05659-5.00036-x

Fundamentals of Feto-Neonatal Immunology

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