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Immunology

D-Index
53
Citations
13422
World Ranking
3946
National Ranking
346

Overview

Peter J. L. Lane is affiliated with the University of Birmingham in the United Kingdom. Their research activity spans several fields within medicine, primarily focusing on infectious diseases, neurology, immunology, nephrology, and pulmonary and respiratory medicine.

Their main research topics include:

  • COVID-19 Clinical Research Studies
  • Long-Term Effects of COVID-19
  • Immunodeficiency and Autoimmune Disorders
  • Renal Diseases and Glomerulopathies
  • Vasculitis and related conditions
  • Systemic Lupus Erythematosus Research

Peter J. L. Lane has contributed to multiple publications, with key recent papers including:

  • "Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK," published in 2022 in Clinical & Experimental Immunology
  • "Blockade of tumor necrosis factor superfamily members CD30 and OX40 abrogates disease activity in murine immune-mediated glomerulonephritis," published in 2021 in Kidney International

Frequent publication venues for their work include:

  • Clinical & Experimental Immunology
  • Kidney International

Collaborations feature several recurring co-authors, such as:

  • Adrian Shields
  • Ariharan Anantharachagan
  • Gururaj Arumugakani
  • Kenneth F. Baker
  • Sameer Bahal

Peter J. L. Lane's research integrates clinical and immunological perspectives, bridging the study of infectious agents like SARS-CoV-2 with autoimmune and renal diseases. This multidisciplinary approach supports investigations into both acute infection outcomes and chronic pathological processes related to immune system dysfunction.

Best Publications

  • Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation.

    M Cella;D Scheidegger;K Palmer-Lehmann;P Lane

  • Sites of specific B cell activation in primary and secondary responses to T cell-dependent and T cell-independent antigens.

    Yong-Jun Liu;Jun Zhang;Peter J. L. Lane;Eric Y.-T. Chan

  • RANK signals from CD4+3− inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla

    Simona W. Rossi;Mi-Yeon Kim;Andreas Leibbrandt;Sonia M. Parnell

  • CD4 T Cell Cytokine Differentiation: The B Cell Activation Molecule, OX40 Ligand, Instructs CD4 T Cells to Express Interleukin 4 and Upregulates Expression of the Chemokine Receptor, Blr-1

    Sarah Flynn;Kai-Michael Toellner;Chandra Raykundalia;Margaret Goodall

  • Activated human T cells express a ligand for the human B cell‐associated antigen CD40 which participates in T cell‐dependent activation of B lymphocytes

    Peter Lane;André Traunecker;Sabine Hubele;Seiji Inui

  • Compromised Ox40 Function in Cd28-Deficient Mice Is Linked with Failure to Develop Cxc Chemokine Receptor 5–Positive Cd4 Cells and Germinal Centers

    Lucy S.K. Walker;Adam Gulbranson-Judge;Sarah Flynn;Thomas Brocker

  • CD4(+)CD3(-) accessory cells costimulate primed CD4 T cells through OX40 and CD30 at sites where T cells collaborate with B cells.

    Mi-Yeon Kim;Fabrina M.C Gaspal;Helen E Wiggett;Fiona M McConnell

  • Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

    Pierre Quartier;Jacinta Bustamante;Ozden Sanal;Alessandro Plebani

  • CD23: a multi-functional receptor/ lymphokine?

    J. Gordon;L. Flores-Romo;J.A. Caims;M.J. Millsum

  • OX40, OX40L and Autoimmunity: a Comprehensive Review

    Gwilym J. Webb;Gwilym J. Webb;Gideon M. Hirschfield;Peter J. L. Lane

  • CD4 T cell traffic control: in vivo evidence that ligation of OX40 on CD4 T cells by OX40-ligand expressed on dendritic cells leads to the accumulation of CD4 T cells in B follicles.

    Thomas Brocker;Adam Gulbranson-Judge;Sarah Flynn;Mireille Riedinger

  • Generating intrathymic microenvironments to establish T-cell tolerance

    Graham Anderson;Peter J. L. Lane;Eric J. Jenkinson

  • The Evolution of B-Cell Clones

    I. C. M. MacLennan;Y. J. Liu;S. Oldfield;J. Zhang

  • Salmonella induces a switched antibody response without germinal centers that impedes the extracellular spread of infection.

    Adam F. Cunningham;Fabrina Gaspal;Karine Serre;Elodie Mohr

  • The thymic medulla is required for Foxp3+ regulatory but not conventional CD4+ thymocyte development.

    Jennifer E. Cowan;Sonia M. Parnell;Kyoko Nakamura;Jorge H. Caamano

  • Role of Ox40 Signals in Coordinating Cd4 T Cell Selection, Migration, and Cytokine Differentiation in T Helper (Th)1 and Th2 Cells

    Peter Lane

  • Mice Deficient in OX40 and CD30 Signals Lack Memory Antibody Responses because of Deficient CD4 T Cell Memory

    Fabrina M. C. Gaspal;Mi-Yeon Kim;Fiona M. McConnell;Chandra Raykundalia

  • Rank Signaling Links the Development of Invariant γδ T Cell Progenitors and Aire+ Medullary Epithelium

    Natalie A. Roberts;Andrea J. White;William E. Jenkinson;Gleb Turchinovich;Gleb Turchinovich

  • Is rapid proliferation in B centroblasts linked to somatic mutation in memory B cell clones

    Jun Zhang;Ian C.M. MacLennan;Yong-Jun Liu;Peter J.L. Lane

  • Generation of both cortical and Aire+ medullary thymic epithelial compartments from CD205+ progenitors

    Song Baik;Eric J. Jenkinson;Peter J. L. Lane;Graham Anderson

Frequent Co-Authors

Graham Anderson
Graham Anderson University of Birmingham
David R. Withers
David R. Withers University of Birmingham
Eric J. Jenkinson
Eric J. Jenkinson University of Birmingham
Ian C. M. MacLennan
Ian C. M. MacLennan University of Birmingham
Jorge Caamano
Jorge Caamano University of Birmingham
Lucy S. K. Walker
Lucy S. K. Walker University College London
Yong-Jun Liu
Yong-Jun Liu University of Washington
Adam F. Cunningham
Adam F. Cunningham University of Birmingham
Hideo Yagita
Hideo Yagita Juntendo University
Josef M. Penninger
Josef M. Penninger University of British Columbia

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