5-year-old male intact rhesus macaque, (Macaca mulatta).This monkey was inoculated with SIVmac251 and was started on combined anti retroviral treatment (CART) 2 months following inoculation. CD 8 depletion was performed on days 6, 8, and 12 post infection.
The animal was in thin body condition and alopecia was present over the neck and back.Â The lungs were mottled, firm and partially collapsed with the left more affected than the right.Â The small intestine was multifocally thickened.Â
Lung: Within the lung parenchyma, there are multifocal to coalescing areas (50 % of total area) of inflammation composed of a mixed population of foamy macrophages, histiocytes, multi-nucleated giant cells, and few numbers of neutrophils, lymphocytes, and plasma cells.Â Interspersed with these areas of inflammation is marked type II pneumocyte hyperplasia that often protrudes into and obscures affected alveolar lumina.Â Additionally, alveoli frequently contain foamy macrophages that are admixed with proteinaceous fluid (edema).Â The multinucleate cells are abundant in many areas and often contain up to 25 irregularly spaced nuclei.Â Often interspersed with the areas of inflammation are aggregates of non-degenerate neutrophils and macrophages in which the macrophages often are cytomegalic with marked karyomegaly and intranuclear eosinophilic inclusion bodies that measure 15-25 Î¼m in diameter and are surrounded by a clear halo.Â Within large airways are occasional plugs of mucus, degenerate cellular debris, and scattered degenerate neutrophils.Â The pleura is multifocally thickened by fibrosis in several areas.Â
Lung: Multifocal to coalescing severe chronic neutrophilic and histiocytic interstitial pneumonia with giant cells and intranuclear cytomegalovirus inclusions.
SIV giant cell pneumonia with cytomegalovirus infection
Simian acquired immunodeficiency syndrome (SAIDS) is characterized by chronic persistent infection with simian immunodeficiency virus (SIV) along with high viremia, low CD4 titer as well as low anti-SIV antibodies that results in opportunistic infections.(14) These opportunistic infections include cytomegalovirus (CMV), Pneumocystis, Mycobacterium and adenoviral infections.(1)
SIV belongs to genus lentivirus under the family Retroviridae.Â Retrovirus virions are enveloped, 80-100 nm in diameter, and have a unique three-layered structure.Â Innermost is the genome nucleoprotein complex, which includes about 30 molecules of reverse transcriptase, and has helical symmetry.Â This structure is enclosed within an icosahedral capsid, about 60 nm in diameter, which in turn is surrounded by a host cell membrane-derived envelope from which glycoprotein peplomers project.Â The genome is diploid, consisting of an inverted dimer of two molecules of linear positive-sense, single stranded RNA; each monomer is 7-11 kb in size and has a 3'-polyadenylated tail and a 5'-cap; the retrovirus genome is organized into 9 ORFs producing 15 proteins.Â SIV infection causes a spectrum of virally-induced lesions that include enteropathy, lymphocytic interstitial pneumonitis, giant cell pneumonia/lymphadenitis, and SIV encephalitis.Â
Giant cell pneumonia is characterized by multinucleated giant cells that are frequently found in terminal cases of SAIDS.(3) Formation of multinucleated giant cells is not completely defined but requires a myriad of factors including 1) infection with SIV, 2) cytokine elaboration from the multinucleated giant cells, and 3) macrophage infiltration.(2)
Cytomegalovirus (CMV) virions are enveloped, about 150 nm in diameter, and contain an icosahedral nucleocapsid about 100 nm in diameter.Â The genome consists of a single linear molecule of double-stranded DNA, 125-235 kbp in size.Â CMV belongs to the Betaherpesvirinae subfamily of Herpesviridae, under the order Herpesvirales. There are number of cytomegalovirus isolated from non-primates that include Cercopithecine herpesvirus 5 (CeHV-5) in African green monkeys, Cercopithecine herpesvirus 8 (CeHV-8) in rhesus monkeys, Human herpesvirus 5 (HHV-5) in humans, as well as Pongine herpesvirus in chimpanzees, Aotine herpesvirus 1 & Aotine herpesvirus 3 in owl monkeys.Â Betaherpesviruses replicate more slowly than alphaherpesviruses and often produce greatly enlarged cells, hence the designation cytomegalovirus.(16) Cytomegaloviruses infect the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions and are typically accompanied by neutrophilic infiltrates.Â
Another common opportunistic lung infection in immunocompromised rhesus macaques is Pneumocystis.Â Pneumocystis pneumonia (PCP) is one of the most common opportunistic diseases in SAIDS.(1,2) Characteristic pathologic features of PCP include infiltration of inflammatory cells in the lung interstitium, thickened alveolar septa by hyperplastic type II pneumocytes, and foamy exudates in the alveoli.Â Some of these features were present in the submitted case; however, immunohistochemistry for Pneumocystis was negative in this case.Â Since Pneumocystis has a morphology similar to protozoa, it was initially considered as such; however, it is now classified as a fungus because the composition and structure of its cell wall (12,15) and nucleotide sequences are more similar to those of fungi than to those of protozoa.(6,13) Although Pneumocystis organisms are found in many different species of mammals, they are strictly species specific.(7) Some of the more common organisms include: Pneumocystis jirovecii (human), P.Â wakefieldii (rat), P.Â murina (mouse), and P.Â carinii (rhesus macaque).(5) In immunocompetent humans and animals, alveolar macrophages (AMs) protect the hosts against Pneumocystis infection by actively removing this extracellular organism from the alveoli.Â However, AMs from Pneumocystis infected animals are defective in phagocytosis,(4,9) and the number of AMs in humans and animals with PCP is reduced.Â These two defects impair innate immunity against Pneumocystis infection.Â The defect in phagocytosis is correlated to down regulation of mannose receptor on the macrophages.(8) The reduction in alveolar macrophage (AM) number is mainly due to increased rate of apoptosis(10) that is triggered by increased levels of intracellular polyamines(11) which could be due to either increased de novo synthesis and uptake of exogenous polyamines.Â Very little is known about the defect in phagocytosis during PCP.
1.Â Lung: Pneumonia, interstitial, histiocytic, with numerous viral syncytial giant cells.Â
2.Â Lung, alveolar macrophages: Intranuclear viral inclusions, rare.
We thank the contributor for providing this excellent example and thorough analysis of two important entities in non-human primates.Â As noted by the contributor and demonstrated in this case, giant-cell pneumonia is a pathognomonic condition associated with SIV infection, while secondary infection with CMV produces significantly enlarged cells with characteristic intranuclear inclusion bodies.Â Although neutrophilic infiltrates typically accompany CMV infection, they are not a prominent feature in this case.Â The moderator also pointed out several opportunistic infections (in addition to cytomegalovirus, Pneumocystis spp.Â mycobacteriosis, and adenovirus) associated with SIV infection in non-human primates, including Cryptosporidium spp., Shigella spp., Campylobacter spp.Â and Epstein-Barr virus.Â
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