<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Angeletti, Andrea</dc:creator>
  <dc:creator>Scapozza, Leonardo</dc:creator>
  <dc:creator>Cavalli, Andrea</dc:creator>
  <dc:creator>Ghiggeri, Gian Marco</dc:creator>
  <dc:creator>Prunotto, Marco</dc:creator>
  <dc:creator>Moll, Solange</dc:creator>
  <dc:date>2021-09-13</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Macrophages are involved in tissue homeostasis. They participate in inflammatory episodes and are involved in tissue repair. Macrophages are  characterized by a phenotypic heterogeneity and a profound cell plasticity. In the kidney, and more particularly within glomeruli, macrophages are  thought to play a maintenance role that is potentially critical for preserving a normal glomerular structure. Literature on the glomerular macrophage  role in human crescentic glomerulonephritis and renal transplantation rejection with glomerulitis, is sparse. Evidence from preclinical models  indicates that macrophages profoundly modulate disease progression, both in terms of number—where depletion has resulted in a reduced  glomerular lesion—and sub-phenotype—M1 being more profoundly detrimental than M2. This evidence is corroborated by better outcomes in  patients with a lower number of glomerular macrophages. However, due to the very limited biopsy sample size, the type and role of macrophage  subpopulations involved in human proliferative lesions is more difficult to precisely define and synthesize. Therefore, specific biomarkers of  macrophage activation may enhance our ability to assess their role, potentially enabling improved monitoring of drug activity and ultimately  allowing the development of novel therapeutic strategies to target these elusive cellular players.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/319255</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1319255</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319255/files/Cavalli_2021_MDPI_cells.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/cells10030603</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319255</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Cells. - 2021, vol. 10, no. 3, p. 19 p</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Glomerulonephritis</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Macrophages</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Immune nephritis</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Glomerular macrophages in human auto- and allo-immune nephritis</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
