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Gotowe bibliografie tematyczne / Organe lymphoïde tertiaire / Artykuły w czasopismach

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Artykuły w czasopismach na temat „Organe lymphoïde tertiaire”

Autor: Grafiati

Data publikacji: 7 grudnia 2024

Data aktualizacji: 31 lipca 2025

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1

Shomer, Nirah H., James G. Fox, Amy E. Juedes, and Nancy H. Ruddle. "Helicobacter-Induced Chronic Active Lymphoid Aggregates Have Characteristics of Tertiary Lymphoid Tissue." Infection and Immunity 71, no. 6 (2003): 3572–77. http://dx.doi.org/10.1128/iai.71.6.3572-3577.2003.

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ABSTRACT Susceptible strains of mice that are naturally or experimentally infected with murine intestinal helicobacter species develop hepatic inflammatory lesions that have previously been described as chronic active hepatitis. The inflammatory infiltrates in some models of chronic autoimmunity or inflammation resemble tertiary lymphoid organs hypothesized to arise by a process termed lymphoid organ neogenesis. To determine whether hepatic inflammation caused by infection with helicobacter could give rise to tertiary lymphoid organs, we used fluorescence-activated cell sorting, immunohistoche

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2

Barone, Francesca, Saba Nayar, Joana Campos, et al. "IL-22 regulates lymphoid chemokine production and assembly of tertiary lymphoid organs." Proceedings of the National Academy of Sciences 112, no. 35 (2015): 11024–29. http://dx.doi.org/10.1073/pnas.1503315112.

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The series of events leading to tertiary lymphoid organ (TLO) formation in mucosal organs following tissue damage remain unclear. Using a virus-induced model of autoantibody formation in the salivary glands of adult mice, we demonstrate that IL-22 provides a mechanistic link between mucosal infection, B-cell recruitment, and humoral autoimmunity. IL-22 receptor engagement is necessary and sufficient to promote differential expression of chemokine (C-X-C motif) ligand 12 and chemokine (C-X-C motif) ligand 13 in epithelial and fibroblastic stromal cells that, in turn, is pivotal for B-cell recru

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3

Erlich, Emma, Rafael Czepielewski, Shashi Kumar, et al. "B cells drive tertiary lymphoid organ formation in ileal inflammation." Journal of Immunology 208, no. 1_Supplement (2022): 113.18. http://dx.doi.org/10.4049/jimmunol.208.supp.113.18.

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Abstract Crohn’s disease [CD] is one of the two most common forms of inflammatory bowel disease, affecting over half a million Americans. Like many other diseases with chronic inflammation, some patients with CD develop tertiary lymphoid organs [TLO] in areas of the gastrointestinal tract with active disease. TLOs are organized clusters of lymphocytes, similar in structure to secondary lymphoid organs, though they develop after birth and their contribution to pathogenesis in CD, or other diseases, is unclear. We, and others, have also found B cell rich lymphoid aggregates in the mesenteric fat

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4

Ruddle, Nancy H. "Lymphatic vessels and tertiary lymphoid organs." Journal of Clinical Investigation 124, no. 3 (2014): 953–59. http://dx.doi.org/10.1172/jci71611.

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5

Feizi, Neda, Neda Feizi, Gang Zhang, Latha Halesha, Khodor Abou Daya, and Martin H. Oberbarnscheidt. "Tertiary Lymphoid Organs promote allograft rejection." Journal of Immunology 212, no. 1_Supplement (2024): 0321_5062. http://dx.doi.org/10.4049/jimmunol.212.supp.0321.5062.

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Abstract Tertiary lymphoid organs (TLOs) are ectopic lymphoid structures that arise in non-lymphoid tissues and are frequently observed in tissue affected by non-resolving chronic inflammation. If TLOs are beneficial or detrimental in transplantation is controversial. We investigate the role of TLO and LTbR in transplantation by manipulating the LTa-LTbR pathway. Using a mouse allo kidney transplantation model, we found that preformed intragraft TLO are sufficient to precipitate rejection in recipients lacking all secondary lymphoid organs (SLO)(LTbRko). In WT recipients with a complete set of

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6

Kirsh, Andrew L., Sharon L. Cushing, Eunice Y. Chen, Stephen M. Schwartz, and Jonathan A. Perkins. "Tertiary Lymphoid Organs in Lymphatic Malformations." Lymphatic Research and Biology 9, no. 2 (2011): 85–92. http://dx.doi.org/10.1089/lrb.2010.0018.

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7

Goyal, Girija, Lucas Barck, Yunhao Zhai, et al. "Human implantable tertiary lymphoid organs (TLO) for solid tumor therapy: from organ chips to the clinic?" Journal of Immunology 212, no. 1_Supplement (2024): 0731_7312. http://dx.doi.org/10.4049/jimmunol.212.supp.0731.7312.

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Abstract We previously created an in vitro human TLO model from patient-derived, circulating immune cells using organ-on-a-chip devices and 3D culture in extracellular matrix (ECM). B cells in these TLOs express activation induced cytidine deaminase, which is only expressed in lymphoid tissues and is required for class switching and somatic hypermutation (SHM). When challenged by vaccines, these TLO undergo SHM and produce antigen-specific antibodies and CD8 T cells. To model cancer associated TLOs, we integrated human pancreatic and lung cancer cell lines into these TLO Chips to understand ho

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8

Lau, Aden, Susan Lester, Sophia Moraitis, et al. "Tertiary lymphoid organs in recalcitrant chronic rhinosinusitis." Journal of Allergy and Clinical Immunology 139, no. 4 (2017): 1371–73. http://dx.doi.org/10.1016/j.jaci.2016.08.052.

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9

Neyt, Katrijn, Frédéric Perros, Corine H. GeurtsvanKessel, Hamida Hammad, and Bart N. Lambrecht. "Tertiary lymphoid organs in infection and autoimmunity." Trends in Immunology 33, no. 6 (2012): 297–305. http://dx.doi.org/10.1016/j.it.2012.04.006.

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10

Shipman, William D., Dragos C. Dasoveanu, and Theresa T. Lu. "Tertiary lymphoid organs in systemic autoimmune diseases: pathogenic or protective?" F1000Research 6 (February 28, 2017): 196. http://dx.doi.org/10.12688/f1000research.10595.1.

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Tertiary lymphoid organs are found at sites of chronic inflammation in autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis. These organized accumulations of T and B cells resemble secondary lymphoid organs and generate autoreactive effector cells. However, whether they contribute to disease pathogenesis or have protective functions is unclear. Here, we discuss how tertiary lymphoid organs can generate potentially pathogenic cells but may also limit the extent of the response and damage in autoimmune disease.

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11

Goyal, Girija, Jaclyn Long, Oren Levy, and Donald E. Ingber. "Biologically Inspired, iterative engineering of a Human Lymphoid Follicle Chip." Journal of Immunology 200, no. 1_Supplement (2018): 120.34. http://dx.doi.org/10.4049/jimmunol.200.supp.120.34.

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Abstract Organs Chips are microengineered, three-dimensional (3D) in vitro models that simulate organ-level pathophysiology and therapeutic responses with high fidelity. Here, we report the development of an in vitro model of lymphoid follicles seen in germinal centers and sites of chronic inflammation. The Human Lymphoid Follicle Chip was designed to mimic lymph flow through the lymph node as well as its cellular and matrix composition. A subcapsular sinus like channel allows the media to flow around the follicles with a fraction of it flowing through the parenchyma. We provide the first know

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12

Zhang, Xueguang, and Binfeng Lu. "IL-17 initiates tertiary lymphoid organ formation." Cellular & Molecular Immunology 9, no. 1 (2011): 9–10. http://dx.doi.org/10.1038/cmi.2011.48.

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13

Clement, Marc, Kevin Guedj, Francesco Andreata, et al. "Control of the T Follicular Helper–Germinal Center B-Cell Axis by CD8 + Regulatory T Cells Limits Atherosclerosis and Tertiary Lymphoid Organ Development." Circulation 131, no. 6 (2015): 560–70. http://dx.doi.org/10.1161/circulationaha.114.010988.

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Background— The atheromodulating activity of B cells during the development of atherosclerosis is well documented, but the mechanisms by which these cells are regulated have not been investigated. Methods and Results— Here, we analyzed the contribution of Qa-1–restricted CD8 + regulatory T cells to the control of the T follicular helper–germinal center B-cell axis during atherogenesis. Genetic disruption of CD8 + regulatory T cell function in atherosclerosis-prone apolipoprotein E knockout mice resulted in overactivation of this axis in secondary lymphoid organs, led to the increased developme

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14

Frija-Masson, Justine, Clémence Martin, Lucile Regard, et al. "Bacteria-driven peribronchial lymphoid neogenesis in bronchiectasis and cystic fibrosis." European Respiratory Journal 49, no. 4 (2017): 1601873. http://dx.doi.org/10.1183/13993003.01873-2016.

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We aimed to characterise lymphoid neogenesis in bronchiectasis and cystic fibrosis (CF) lungs and to examine the role of bacterial infection.Lymphoid aggregates were examined using immunohistochemical staining and morphometric analysis in surgical lung sections obtained from nonsmokers and patients with bronchiectasis or CF. Sterile, Pseudomonas aeruginosa- or Staphylococcus aureus-coated agarose beads were instilled intratracheally in mice. Kinetics of lymphoid neogenesis and chemokine expression were examined over 14 days.Lymphoid aggregates were scarce in human lungs of nonsmokers, but nume

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15

Bonnan, M. "Organes lymphoïdes tertiaires méningés : des acteurs majeurs de l’auto-immunité intrathécale." Revue Neurologique 171, no. 1 (2015): 65–74. http://dx.doi.org/10.1016/j.neurol.2014.08.003.

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16

Daya, Khodor Abou, Daqiang Zhao, Kyle Biery, and Martin H. Oberbarnscheidt. "Tertiary lymphoid organs in renal chronic allograft rejection." Journal of Immunology 204, no. 1_Supplement (2020): 161.14. http://dx.doi.org/10.4049/jimmunol.204.supp.161.14.

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Abstract Chronic allograft rejection remains a major obstacle to long-term allograft survival. The immunologic role of tertiary lymphoid organs (TLO) in allograft rejection is unclear. Here, we employed a chronic renal allograft rejection model in mice and intravital 2-photon microscopy to investigate the function of TLO in transplant rejection. CB6F1 (F1) RIP-LTα (preformed TLO) or F1 (no TLO) kidney grafts were transplanted to WT B6 recipients and survival monitored. To investigate immunologic function of TLO, we adoptively transferred B6-RIPLTα CD11c-YFP mice with 10m naïve dsRed OT-I T cel

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17

Li, Yanni, Sihe Gong, Kaijie Yan, Zhonghong Shi, Yimin Bao, and Ke Ning. "Artery tertiary lymphoid organs in atherosclerosis: A review." Life Sciences 369 (May 2025): 123549. https://doi.org/10.1016/j.lfs.2025.123549.

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18

Maehara, Takashi, Hamid Mattoo, Vinay S. Mahajan, et al. "The expansion in lymphoid organs of IL-4+ BATF+ T follicular helper cells is linked to IgG4 class switching in vivo." Life Science Alliance 1, no. 1 (2018): e201800050. http://dx.doi.org/10.26508/lsa.201800050.

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Distinct T follicular helper (TFH) subsets that influence specific class-switching events are assumed to exist, but the accumulation of isotype-specific TFH subsets in secondary lymphoid organs (SLOs) and tertiary lymphoid organs has not been hitherto demonstrated. IL-4–expressing TFH cells are surprisingly sparse in human SLOs. In contrast, in IgG4-related disease (IgG4-RD), a disorder characterized by polarized Ig class switching, most TFH cells in tertiary and SLOs make IL-4. Human IL-4+ TFH cells do not express GATA-3 but express nuclear BATF, and the transcriptomes of IL-4–secreting TFH c

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19

Akhavanpoor, Mohammadreza, Christian A. Gleissner, Hamidreza Akhavanpoor, et al. "Adventitial tertiary lymphoid organ classification in human atherosclerosis." Cardiovascular Pathology 32 (January 2018): 8–14. http://dx.doi.org/10.1016/j.carpath.2017.08.002.

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20

Motallebzadeh, R., S. Rehakova, M. Goddard, et al. "ALLOGRAFT TERTIARY LYMPHOID ORGAN DEVELOPMENT REQUIRES HUMORAL IMMUNITY." Transplantation Journal 90 (July 2010): 485. http://dx.doi.org/10.1097/00007890-201007272-00899.

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21

Segerer, S., and D. Schlöndorff. "B cells and tertiary lymphoid organs in renal inflammation." Kidney International 73, no. 5 (2008): 533–37. http://dx.doi.org/10.1038/sj.ki.5002734.

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22

Berteloot, Laureline, Thierry Jo Molina, Julie Bruneau, et al. "Alternative pathways for the development of lymphoid structures in humans." Proceedings of the National Academy of Sciences 118, no. 29 (2021): e2108082118. http://dx.doi.org/10.1073/pnas.2108082118.

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Lymphoid tissue inducer (LTi) cells are critical for inducing the differentiation of most secondary lymphoid organs (SLOs) in mice. In humans, JAK3 and γc deficiencies result in severe combined immunodeficiency (SCIDs) characterized by an absence of T cells, natural killer cells, innate lymphoid cells (ILCs), and presumably LTi cells. Some of these patients have undergone allogeneic stem cell transplantation (HSCT) in the absence of myeloablation, which leads to donor T cell engraftment, while other leukocyte subsets are of host origin. By using MRI to look for SLOs in nine of these patients 1

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23

Nayar, S., J. Campos, T. Cloake, et al. "SAT0005 IL22 Regulates Autoantibody Production by Inducing Lymphoid Chemokine Expression in Tertiary Lymphoid Organs." Annals of the Rheumatic Diseases 74, Suppl 2 (2015): 651.2–651. http://dx.doi.org/10.1136/annrheumdis-2015-eular.5049.

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24

Xu, Xiaoguang, Yong Han, Qiang Wang, et al. "Characterisation of Tertiary Lymphoid Organs in Explanted Rejected Donor Kidneys." Immunological Investigations 45, no. 1 (2015): 38–51. http://dx.doi.org/10.3109/08820139.2015.1085394.

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Ciccia, F., A. Rizzo, R. Alessandro, et al. "SAT0023 Artery Tertiary Lymphoid Organs Occur in Giant Cell Arteritis." Annals of the Rheumatic Diseases 75, Suppl 2 (2016): 672.1–672. http://dx.doi.org/10.1136/annrheumdis-2016-eular.1383.

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26

Pillai, Shiv, and Faisal Alsufyani. "Winning with the B team?" Science Immunology 5, no. 44 (2020): eabb0236. http://dx.doi.org/10.1126/sciimmunol.abb0236.

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27

Rustamkhanov, R. A., K. Sh Gantsev, and D. S. Tursumetov. "Tertiary Lymphoid Structures and Cancer Prognosis (Brief Review)." Creative surgery and oncology 9, no. 4 (2020): 293–96. http://dx.doi.org/10.24060/2076-3093-2019-9-4-293-296.

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This brief review is devoted to the role of tertiary lymphoid structures in oncological processes. A number of research studies carried out over the past ten years have shed light on the functions of such structures in various diseases, as well as their role in the progression of the pathological process or resolution of a disease. The data presented in some research works confirms the relationship between the presence of tumour-specific (tumour-associated) tertiary lymphoid structures and a favourable prognosis in patients with various oncological diseases, which suggests the participation of

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28

Magrone, Thea, and Emilio Jirillo. "Development and Organization of the Secondary and Tertiary Lymphoid Organs: Influence of Microbial and Food Antigens." Endocrine, Metabolic & Immune Disorders - Drug Targets 19, no. 2 (2019): 128–35. http://dx.doi.org/10.2174/1871530319666181128160411.

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Background:Secondary lymphoid organs (SLO) are distributed in many districts of the body and, especially, lymph nodes, spleen and gut-associated lymphoid tissue are the main cellular sites. On the other hand, tertiary lymphoid organs (TLO) are formed in response to inflammatory, infectious, autoimmune and neoplastic events. </P><P> Developmental Studies: In the present review, emphasis will be placed on the developmental differences of SLO and TLO between small intestine and colon and on the role played by various chemokines and cell receptors. Undoubtedly, microbiota is indispensa

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29

Buckley, Christopher D., Francesca Barone, Saba Nayar, Cecile Bénézech, and Jorge Caamaño. "Stromal Cells in Chronic Inflammation and Tertiary Lymphoid Organ Formation." Annual Review of Immunology 33, no. 1 (2015): 715–45. http://dx.doi.org/10.1146/annurev-immunol-032713-120252.

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Jeevanandam, Advait, Kelli Connolly, and Nikhil Joshi. "Abstract B032: Spatial study of tertiary lymphoid structures in lung adenocarcinoma using 3D lightsheet whole-organ Imaging and machine learning-based quantification." Cancer Research 84, no. 22_Supplement (2024): B032. http://dx.doi.org/10.1158/1538-7445.tumbody-b032.

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Abstract Lung Adenocarcinoma (LUAD) leads in cancer deaths worldwide. Immune Checkpoint blockade (ICB) therapy has improved patient survival of some subtypes (like Kras oncogene-driven; loss of tumor-suppressor p53– “KP”), but not others (Kras oncogene-driven; loss of LKB1– “KL”). Some studies suggest the poorly inflamed KL tumor environment reduces T cell infiltration. However, the impact of other immune mechanisms/cell types on overall ICB-responsiveness remains understudied. Tertiary lymphoid structures (TLSs) are T/B cell aggregates organized by various cell types that form within inflamed

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31

Adoke, Kasimu, and Sanusi Haruna. "10 Tertiary lymphoid structure in pancreatic ductal adenocarcinoma; a potential target in an immunologically inert malignancy." Journal for ImmunoTherapy of Cancer 9, Suppl 2 (2021): A10. http://dx.doi.org/10.1136/jitc-2021-sitc2021.010.

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BackgroundTertiary lymphoid structure (TLS) are immune aggregates with various degrees of organization that forms outside of secondary lymphoid organ in response to chronic inflammation, infection or tumours.1 2 TLS like secondary lymphoid organ, has defined T cell zones, B cell zones, high endothelial venules (HEV) and matured dendritic cells. They have been shown to correlate with increase patient survival in many tumours. Pancreatic ductal carcinoma (PDAC) is generally believed to be immunologically inert, low tumour mutation burden (TMB) and poor response to checkpoint blockade. Recent fin

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32

Deng, Shuzhe, Xinxin Yang, Lin He, Yunjing Hou, and Hongxue Meng. "Tertiary Lymphoid Structures in Microorganism-Related Cancer." Cancers 16, no. 20 (2024): 3464. http://dx.doi.org/10.3390/cancers16203464.

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Tertiary lymphoid structures (TLSs) are ectopic lymphoid tissues formed by the accumulation of lymphocytes and other components outside lymphoid organs. They have been shown to be widespread in cancers and have predictive effects on prognosis and immunotherapy efficacy; however, there is no standardized measurement guide. This paper provides a reference for future research. Moreover, the induction strategy for the formation mechanism of TLSs is a new direction for future cancer treatment, such as cancer vaccines for microorganisms. The effects of microorganisms on cancer are dual. The role of

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33

Thaunat, Olivier, Natacha Patey, Chantal Gautreau, et al. "B Cell Survival in Intragraft Tertiary Lymphoid Organs After Rituximab Therapy." Transplantation 85, no. 11 (2008): 1648–53. http://dx.doi.org/10.1097/tp.0b013e3181735723.

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Paramasivan, Sathish, Susan Lester, Aden Lau, et al. "Tertiary lymphoid organs: A novel target in patients with chronic rhinosinusitis." Journal of Allergy and Clinical Immunology 142, no. 5 (2018): 1673–76. http://dx.doi.org/10.1016/j.jaci.2018.07.024.

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Nasr, Isam W., Qi Li, and Fadi G. Lakkis. "Inhibition of tertiary lymphoid organs in a murine chronic rejection model." Journal of the American College of Surgeons 209, no. 3 (2009): S57—S58. http://dx.doi.org/10.1016/j.jamcollsurg.2009.06.137.

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Schaadt, Nadine S., Ralf Schönmeyer, Germain Forestier, et al. "Graph-based description of tertiary lymphoid organs at single-cell level." PLOS Computational Biology 16, no. 2 (2020): e1007385. http://dx.doi.org/10.1371/journal.pcbi.1007385.

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Thelen, M., MA García-Márquez, T. Nestler, et al. "P03.03 Organization, function and gene expression of tertiary lymphoid structures in PDAC resembles lymphoid follicles in secondary lymphoid organs." Journal for ImmunoTherapy of Cancer 8, Suppl 2 (2020): A23.1—A23. http://dx.doi.org/10.1136/jitc-2020-itoc7.43.

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BackgroundSecondary lymphoid organs (SLO) are involved in induction and enhancement of anti-tumor immune responses on different tumor entities. Recent evidence suggests that anti-tumor immune responses may also be induced or enhanced in the tumor microenvironment in so called tertiary lymphoid structures (TLS). It is assumed that TLS represent a hotspot for T cell priming, B cell activation, and differentiation, leading to cellular and humoral anti-tumor immune response.MethodsFFPE-slides of 120 primary pancreatic ductal adenocarcinoma (PDAC) patients were immunohistochemically (IHC) stained f

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38

Pei, Guangchang, Rui Zeng, Min Han, et al. "Renal Interstitial Infiltration and Tertiary Lymphoid Organ Neogenesis in IgA Nephropathy." Clinical Journal of the American Society of Nephrology 9, no. 2 (2013): 255–64. http://dx.doi.org/10.2215/cjn.01150113.

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Frasca, Daniela, and Bonnie B. Blomberg. "Adipose Tissue: A Tertiary Lymphoid Organ: Does It Change with Age?" Gerontology 66, no. 2 (2019): 114–21. http://dx.doi.org/10.1159/000502036.

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Mounzer, Rawad H., Oyvind S. Svendsen, Peter Baluk, et al. "Lymphotoxin-alpha contributes to lymphangiogenesis." Blood 116, no. 12 (2010): 2173–82. http://dx.doi.org/10.1182/blood-2009-12-256065.

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Abstract Lymphotoxin-α (LTα), lymphotoxin-β (LTβ), and tumor necrosis factor-α (TNFα) are inflammatory mediators that play crucial roles in lymphoid organ development. We demonstrate here that LTα also contributes to the function of lymphatic vessels and to lymphangiogenesis during inflammation. LTα−/− mice exhibited reduced lymph flow velocities and increased interstitial fluid pressure. Airways of LTβ−/− mice infected with Mycoplasma pulmonis had significantly more lymphangiogenesis than wild type (WT) or LTα−/− mice, as did the skin draining immunization sites of LTβ−/− mice. Macrophages, B

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41

Lu, Theresa T., Hajeong Kim, and Xiaojing Ma. "IL-17, a new kid on the block of tertiary lymphoid organs." Cellular & Molecular Immunology 9, no. 1 (2011): 3–4. http://dx.doi.org/10.1038/cmi.2011.34.

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Huang, Hsin-Ying, and Sanjiv A. Luther. "Expression and function of interleukin-7 in secondary and tertiary lymphoid organs." Seminars in Immunology 24, no. 3 (2012): 175–89. http://dx.doi.org/10.1016/j.smim.2012.02.008.

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Wirsing, A., O. Rikardsen, S. E. Steigen, L. Uhlin-Hansen, and E. Hadler-Olsen. "886: Prognostic relevance of tertiary lymphoid organs in oral squamous cell carcinoma." European Journal of Cancer 50 (July 2014): S216. http://dx.doi.org/10.1016/s0959-8049(14)50786-1.

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Zhai, Yunhao, Pranav Prabhala, Lucas Barck, et al. "Abstract B063: Tertiary lymphoid organogenesis and lymphocyte activation in human organ chips." Cancer Research 84, no. 2_Supplement (2024): B063. http://dx.doi.org/10.1158/1538-7445.panca2023-b063.

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Abstract The rates of tertiary lymphoid organ (TLO) formation in pancreatic cancer are very low but patients with TLO have dramatically better survival rates. Our goal is to understand how pancreatic cancer suppresses TLO so that we can improve patient survival and reduce recurrence. We integrated human cell lines from pancreatic and lung cancer with either high or low PDL1/L2 expression into our previously described lymphoid follicle (LF) chip (Goyal et al., Adv. Sci, 2022), where peripheral blood mononuclear cells are induced to form 3D TLO-like structures. The hot lung cancer cell line, whi

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45

Galy, A., M. Clément, P. Bruneval, et al. "Organes lymphoïdes tertiaires dans l’artérite de Takayasu : les lymphocytes B sont-ils impliqués dans la pathogénie ?" La Revue de Médecine Interne 37 (June 2016): A106. http://dx.doi.org/10.1016/j.revmed.2016.04.046.

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Weiss, J. M., P. Cufi, R. Le Panse, and S. Berrih-Aknin. "The thymus in autoimmune Myasthenia Gravis: Paradigm for a tertiary lymphoid organ." Revue Neurologique 169, no. 8-9 (2013): 640–49. http://dx.doi.org/10.1016/j.neurol.2013.02.005.

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Reed, Hasina Outtz, Liqing Wang, Jarrod Sonett, et al. "Lymphatic impairment leads to pulmonary tertiary lymphoid organ formation and alveolar damage." Journal of Clinical Investigation 129, no. 6 (2019): 2514–26. http://dx.doi.org/10.1172/jci125044.

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Műzes, Györgyi, Bettina Bohusné Barta, and Ferenc Sipos. "Colitis and Colorectal Carcinogenesis: The Focus on Isolated Lymphoid Follicles." Biomedicines 10, no. 2 (2022): 226. http://dx.doi.org/10.3390/biomedicines10020226.

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Gut-associated lymphoid tissue is one of the most diverse and complex immune compartments in the human body. The subepithelial compartment of the gut consists of immune cells of innate and adaptive immunity, non-hematopoietic mesenchymal cells, and stem cells of different origins, and is organized into secondary (and even tertiary) lymphoid organs, such as Peyer’s patches, cryptopatches, and isolated lymphoid follicles. The function of isolated lymphoid follicles is multifaceted; they play a role in the development and regeneration of the large intestine and the maintenance of (immune) homeost

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Sunyer, J. Oriol, Yasuhiro Shibasali, Fumio Takizawa, Ding Yang, Pierre Boudinot, and Aleksei Krasnov. "IDENTIFICATION OF PRIMORDIAL ORGANIZED LYMPHOID STRUCTURE IN THE SPLEEN OF TELEOST FISH." Journal of Immunology 204, no. 1_Supplement (2020): 92.40. http://dx.doi.org/10.4049/jimmunol.204.supp.92.40.

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Abstract Induction of adaptive immune responses in higher vertebrate species occur within organized lymphoid structures (e.g. lymph nodes, Peyer’s patches). It has been proposed that such structures emerged throughout evolutionary time with the goal to maximize encounters between antigens, antigens-presenting cells and B-T lymphocytes. Fish lack such structures and thus, it remains unknown how and where antigen-specific immunoglobulin responses are induced in these species. To understand how systemic immune responses are induced in teleost lymphoid organs, Rainbow Trout were immunized with sev

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Willard-Mack, Cynthia L., Susan A. Elmore, William C. Hall, et al. "Nonproliferative and Proliferative Lesions of the Rat and Mouse Hematolymphoid System." Toxicologic Pathology 47, no. 6 (2019): 665–783. http://dx.doi.org/10.1177/0192623319867053.

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The INHAND Project (International Harmonization of Nomenclature and Diagnostic Criteria for Lesions in Rats and Mice) is a joint initiative of the Societies of Toxicologic Pathology from Europe (ESTP), Great Britain (BSTP), Japan (JSTP), and North America (STP) to develop an internationally accepted nomenclature for proliferative and nonproliferative changes in rats and mice. The purpose of this publication is to provide a standardized nomenclature for classifying changes observed in the hematolymphoid organs, including the bone marrow, thymus, spleen, lymph nodes, mucosa-associated lymphoid t

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