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3.
J Med Virol ; 91(9): 1577-1583, 2019 09.
Article in English | MEDLINE | ID: mdl-31090222

ABSTRACT

The emergence of Zika virus in the Americas has caused an increase of babies born with microcephaly or other neurological malformations. The differential diagnosis of Zika infection, particularly serological diagnosis, is an important but complex issue. In this study, we describe clinical manifestations of 94 suspected cases of congenital Zika from Bahia state, Brazil, and the results of serological tests performed on children and/or their mothers at an average of 71 days after birth. Anti-Zika immunoglobulin M (IgM) antibodies were detected in 44.4% and in 7.1% of samples from mothers and children, respectively. Nearly all the IgM, and 92% of immunoglobulin G positive results were confirmed by neutralization test. Zika specific neutralizing antibodies were detected in as much as 90.4% of the cases. Moreover, dengue specific neutralizing antibodies were detected in 79.0% of Zika seropositive mothers. In conclusion, Zika IgM negative results should be considered with caution, due to a possible rapid loss of sensitivity after birth, while the NS1-based Zika IgM enzyme-linked immunosorbent assay test we have used has demonstrated to be highly specific. In a high percentage of cases, Zika specific neutralizing antibodies were detected, which are indicative of a past Zika infection, probably occurred during pregnancy in this population.


Subject(s)
Infectious Disease Transmission, Vertical/statistics & numerical data , Zika Virus Infection/epidemiology , Zika Virus Infection/transmission , Zika Virus , Adult , Antibodies, Neutralizing/blood , Antibodies, Viral/blood , Brazil/epidemiology , Child, Preschool , Diagnostic Imaging , Humans , Immunoglobulin M/blood , Infant , Infant, Newborn , Neutralization Tests , Phenotype , Public Health Surveillance , Serologic Tests , Zika Virus Infection/diagnosis
4.
J Med Virol ; 90(10): 1666-1668, 2018 10.
Article in English | MEDLINE | ID: mdl-29797606

ABSTRACT

A collection of 3069 human sera collected in the area of the municipality of Modena, Emilia Romagna, Italy, was retrospectively investigated for specific antibodies against Usutu (USUV) and West Nile viruses (WNV). All the samples resulting positive using a preliminary screening test were analyzed with the plaque reduction neutralization test. Overall, 24 sera were confirmed as positive for USUV (0.78%) and 13 for WNV (0.42%). The results suggest that in 2012, USUV was circulating more than WNV in North-eastern Italy.


Subject(s)
Antibodies, Viral/blood , Flavivirus/immunology , West Nile virus/immunology , Antibodies, Neutralizing/blood , Blood Donors , Humans , Italy/epidemiology , Neutralization Tests , Retrospective Studies , Seroepidemiologic Studies
5.
Euro Surveill ; 23(22)2018 05.
Article in English | MEDLINE | ID: mdl-29871722

ABSTRACT

We compared the vector competence of an Italian population of Aedes albopictus for two strains of chikungunya virus (CHIKV), with and without E1:A226V mutation, responsible for outbreaks in 2007 in the Emilia Romagna region and 2017 in the Lazio and Calabria regions, respectively. Ae. albopictus showed similar vector competence for both viral strains indicating that E1:A226V mutation is not exclusively responsible for ability of CHIKV to replicate well in this mosquito species.


Subject(s)
Aedes/virology , Alphavirus Infections/transmission , Chikungunya Fever/virology , Chikungunya virus/genetics , Chikungunya virus/pathogenicity , Mosquito Vectors/virology , Mutation/genetics , Aedes/physiology , Alphavirus Infections/epidemiology , Animals , Chikungunya Fever/diagnosis , Chikungunya Fever/epidemiology , Chikungunya virus/isolation & purification , Disease Outbreaks , Disease Vectors , Humans , Indian Ocean , Italy/epidemiology , Mosquito Vectors/physiology , RNA, Viral/analysis , Species Specificity
6.
Med Lav ; 109(2): 125-131, 2018 01 30.
Article in English | MEDLINE | ID: mdl-29701628

ABSTRACT

BACKGROUND: Arthropod-borne viruses (Arbovirus) play an important role among emerging and re-emerging infectious diseases and in the spreading of infections in new geographic areas. Although some arboviral infections may be asymptomatic or mild flu-like illnesses, many occur as severe forms of meningitis and meningoencephalitis. OBJECTIVES: To assess whether arboviral infections may be associated with occupational risk, in a population of agricultural and forestry workers potentially at high risk for arthropods bite and sting. METHODS: A seroprevalence survey for arboviruses belonging to the genera Flaviviruses (West Nile, Tick-borne encephalitis and Usutu viruses) and Phlebovirus (Toscana virus) was carried out in Grosseto province (Tuscany, Italy). One hundred and one serum samples of occupationally exposed workers and 100 serum samples of not exposed workers were analyzed using commercial and home-made serological assays. Serological data were obtained in 2012 and analyzed according to demographic characteristics, recollection of insect-bites, and time spent in outdoor activities. RESULTS: A total seropositivity of 10% (21/201) was observed for Toscana virus. No difference in seroprevalence for Toscana virus was observed among the exposed (10/101) versus the not exposed (11/100) workers. No seropositivity for West Nile, Usutu and Tick-borne encephalitis viruses was detected. CONCLUSIONS: Although circulation of Toscana virus is recognized in the study area, our results did not reveal a higher risk for workers exposed to arthropods bite and sting. Health surveillance programs remain useful to monitor the potential emergence of arboviruses.


Subject(s)
Agriculture/statistics & numerical data , Arbovirus Infections/epidemiology , Occupational Diseases/epidemiology , Occupational Exposure/adverse effects , Adult , Animals , Arbovirus Infections/blood , Arbovirus Infections/virology , Arboviruses/isolation & purification , Encephalitis, Tick-Borne/epidemiology , Female , Humans , Italy/epidemiology , Male , Middle Aged , Occupational Diseases/blood , Occupational Diseases/virology , Population Surveillance , Prevalence , Retrospective Studies , Risk Factors , Seroepidemiologic Studies , Surveys and Questionnaires , Ticks
7.
BMC Infect Dis ; 17(1): 216, 2017 03 16.
Article in English | MEDLINE | ID: mdl-28302072

ABSTRACT

BACKGROUND: Imported cases of infections due to Dengue (DENV) and Chikungunya (CHIKV) viruses and, more recently, Zika virus (ZIKV) are commonly reported among travelers returning from endemic regions. In areas where potentially competent vectors are present, the risk of autochthonous transmission of these vector-borne pathogens is relatively high. Laboratory surveillance is crucial to rapidly detect imported cases in order to reduce the risk of transmission. This study describes the laboratory activity performed by the National Reference Laboratory for Arboviruses (NRLA) at the Italian National Institute of Health in the period from July 2014 to October 2015. METHODS: Samples from 180 patients visited/hospitalized with a suspected DENV/CHIKV/ZIKV infection were sent to the NRLA from several Italian Hospitals and from Regional Reference Laboratories for Arboviruses, in agreement with the National Plan on human surveillance of vector-borne diseases. Both serological (ELISA IgM test and Plaque Reduction Neutralization Test-PRNT) and molecular assays (Real Time PCR tests, RT-PCR plus nested PCR and sequencing of positive samples) were performed. RESULTS: DENV infection was the most frequently diagnosed (80 confirmed/probable cases), and all four genotypes were detected. However, an increase in imported CHIKV cases (41 confirmed/probable cases) was observed, along with the detection of the first ZIKV cases (4 confirmed cases), as a consequence of the recent spread of both CHIKV and ZIKV in the Americas. CONCLUSIONS: Main diagnostic issues highlighted in our study are sensitivity limitations of molecular tests, and the importance of PRNT to confirm serological results for differential diagnosis of Arboviruses. The continuous evaluation of diagnostic strategy, and the implementation of laboratories networks involved in surveillance activities is essential to ensure correct diagnosis, and to improve the preparedness for a rapid and proper identification of viral threats.


Subject(s)
Chikungunya Fever/diagnosis , Chikungunya virus/isolation & purification , Dengue Virus/isolation & purification , Dengue/diagnosis , Molecular Diagnostic Techniques/methods , Zika Virus Infection/diagnosis , Zika Virus/isolation & purification , Chikungunya Fever/epidemiology , Chikungunya Fever/genetics , Chikungunya Fever/transmission , Chikungunya virus/genetics , Dengue/epidemiology , Dengue/genetics , Dengue/transmission , Dengue Virus/genetics , Disease Outbreaks/prevention & control , Female , Genotype , Humans , Italy/epidemiology , Male , Population Surveillance , Public Health , Travel , Young Adult , Zika Virus/genetics , Zika Virus Infection/epidemiology , Zika Virus Infection/prevention & control , Zika Virus Infection/transmission
8.
Euro Surveill ; 22(39)2017 Sep.
Article in English | MEDLINE | ID: mdl-29019306

ABSTRACT

An autochthonous chikungunya outbreak is ongoing near Anzio, a coastal town in the province of Rome. The virus isolated from one patient and mosquitoes lacks the A226V mutation and belongs to an East Central South African strain. As of 20 September, 86 cases are laboratory-confirmed. The outbreak proximity to the capital, its late summer occurrence, and diagnostic delays, are favouring transmission. Vector control, enhanced surveillance and restricted blood donations are being implemented in affected areas.


Subject(s)
Aedes/virology , Chikungunya Fever/diagnosis , Chikungunya virus/genetics , Chikungunya virus/isolation & purification , Disease Outbreaks , Animals , Antibodies, Viral , Chikungunya Fever/epidemiology , Chikungunya Fever/prevention & control , Disease Outbreaks/prevention & control , Female , Humans , Insect Vectors/virology , Italy/epidemiology , Phylogeny , Polymerase Chain Reaction , Viral Envelope Proteins/genetics
9.
Euro Surveill ; 21(8): 30148, 2016.
Article in English | MEDLINE | ID: mdl-26939607

ABSTRACT

We report a case of Zika virus infection imported in Florence, Italy ex-Thailand, leading to a secondary autochthonous case, probably through sexual transmission. The two cases occurred in May 2014 but were retrospectively diagnosed in 2016 on the basis of serological tests (plaque reduction neutralisation) performed on stored serum samples. Our report provides further evidence that sexual transmission of Zika virus is possible.


Subject(s)
Coitus , Travel , Zika Virus Infection/diagnosis , Zika Virus Infection/transmission , Zika Virus/isolation & purification , Adult , Exanthema/virology , Female , Humans , Italy , Male , Pregnancy , RNA, Viral/blood , Serologic Tests , Thailand , Zika Virus Infection/virology
10.
Euro Surveill ; 21(18)2016 May 05.
Article in English | MEDLINE | ID: mdl-27171034

ABSTRACT

We report a study on vector competence of an Italian population of Aedes albopictus for Zika virus (ZIKV). Ae. albopictus was susceptible to ZIKV infection (infection rate: 10%), and the virus could disseminate and was secreted in the mosquito's saliva (dissemination rate: 29%; transmission rate: 29%) after an extrinsic incubation period of 11 days. The observed vector competence was lower than that of an Ae. aegypti colony tested in parallel.


Subject(s)
Aedes/virology , Animal Structures/virology , Mosquito Vectors/virology , Saliva/virology , Zika Virus Infection/virology , Zika Virus/isolation & purification , Animals , Female , Humans , Italy , Viral Load , Zika Virus/pathogenicity
11.
Euro Surveill ; 21(35)2016 Sep 01.
Article in English | MEDLINE | ID: mdl-27605056

ABSTRACT

We investigated the susceptibility of an Italian population of Culex pipiens mosquitoes to Zika virus (ZIKV) infection, tested in parallel with Aedes aegypti, as a positive control. We analysed mosquitoes at 0, 3, 7, 10, 14, 20 and 24 days after an infectious blood meal. Viral RNA was detected in the body of Cx. pipiens up to three days post-infection, but not at later time points. Our results indicate that Cx. pipiens is not susceptible to ZIKV infection.


Subject(s)
Aedes/virology , Culex/virology , Insect Vectors/virology , Zika Virus Infection/transmission , Zika Virus/isolation & purification , Zika Virus/pathogenicity , Animals , Disease Susceptibility , Female , Real-Time Polymerase Chain Reaction , Viral Load , Zika Virus/genetics , Zika Virus Infection/virology
14.
Immunol Cell Biol ; 89(3): 437-46, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20805841

ABSTRACT

Mycobacterium tuberculosis (Mtb) evades the immune response by impairing the functions of different antigen-presenting cells. We have recently shown that Mtb hijacks differentiation of monocytes into dendritic cells (DCs). To further characterize the mechanisms underlying this process, we investigated the consequences of inducing dendritic cell differentiation using interferon-α and granulocyte-macrophage colony-stimulating factor in the presence of supernatants (SNs) obtained from monocyte cultures treated with or without heat-inactivated Mtb. Although the SNs from control cultures do not interfere with the generation of fully differentiated DCs, monocytes stimulated with SNs from Mtb-stimulated cells (SN Mtb) remained CD14(+) and poorly differentiated into CD1a(+) cells. Among cytokines known to affect dendritic cell differentiation, we observed a robust production of interleukin-1ß, interleukin-6, interleukin-10 and tumor necrosis factor-α upon Mtb stimulation. However, only interleukin-10 neutralization through the addition of soluble interleukin-10 receptor reversed the inhibitory activity of SN Mtb. Accordingly, the addition of recombinant interleukin-10 was able to significantly reduce CD1a expression. The interaction of Mtb with differentiating monocytes rapidly activates p38 mitogen-activated protein kinase, signal transducer and activator of transcription pathways, which are likely involved in interleukin-10 gene expression. Taken together, our results suggest that Mtb may inhibit the differentiation of bystander non-infected monocytes into DCs through the release of interleukin-10. These results shed light on new aspects of the host-pathogen interaction, which might help to identify innovative immunological strategies to limit Mtb virulence.


Subject(s)
Bystander Effect , Cell Differentiation , Dendritic Cells/cytology , Dendritic Cells/immunology , Interleukin-10/immunology , Mycobacterium tuberculosis/physiology , Tuberculosis/immunology , Bystander Effect/immunology , Cell Differentiation/drug effects , Cell Differentiation/immunology , Culture Media, Conditioned/chemistry , Culture Media, Conditioned/pharmacology , Cytokines/biosynthesis , Humans , Interferon-alpha/immunology , Interferon-alpha/metabolism , Monocytes/immunology , Monocytes/metabolism , Mycobacterium tuberculosis/immunology , STAT3 Transcription Factor/metabolism , Signal Transduction/drug effects , Signal Transduction/immunology , p38 Mitogen-Activated Protein Kinases/metabolism
15.
Clin Dev Immunol ; 2011: 841346, 2011.
Article in English | MEDLINE | ID: mdl-21197399

ABSTRACT

Knowledge of the molecular events regulating the innate response to Mycobacterium tuberculosis (Mtb) is critical for understanding immunological pathogenesis and protection from tuberculosis. To this aim, the regulation and the expression of regulatory and proinflammatory cytokines were investigated in human primary monocytes upon Mtb infection. We found that Mtb-infected monocytes preferentially express a proinflammatory cytokine profile, including IL-6, TNF-α, and IL-1ß. Conversely, among the regulatory cytokines, Mtb elicited IL-10 and IL-23 release while no expression of IL-12p70, IL-27, and IFN-ß was observed. The analysis of the signalling pathways leading to this selective cytokine expression showed that in monocytes Mtb activates MAPK and NF-κB but is unable to stimulate IRF-3 phosphorylation, a transcription factor required for IL-12p35 and IFN-ß gene expression. Thus, by inducing a specific cytokine profile, Mtb can influence the immunoregulatory properties of monocytes, which represent important target of novel vaccinal strategies against Mtb infection.


Subject(s)
Cytokines , Gene Expression , Monocytes , Cell Culture Techniques , Cytokines/genetics , Cytokines/immunology , Cytokines/metabolism , Gene Expression/immunology , Humans , Interferon Regulatory Factor-3/immunology , Interferon Regulatory Factor-3/metabolism , MAP Kinase Signaling System/immunology , Monocytes/immunology , Monocytes/metabolism , Monocytes/microbiology , Mycobacterium tuberculosis/immunology , Mycobacterium tuberculosis/metabolism , NF-kappa B/immunology , NF-kappa B/metabolism , Phosphorylation , Signal Transduction/genetics , Signal Transduction/immunology , Th1-Th2 Balance
16.
Mol Cell Neurosci ; 45(3): 234-44, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20600925

ABSTRACT

Fine regulation of the innate immune response following brain injury or infection is important to avoid excessive activation of microglia and its detrimental consequences on neural cell viability and function. To get insights on the molecular networks regulating microglia activation, we analyzed expression, regulation and functional relevance of tumor necrosis factor receptors (TNFR) 2 in cultured mouse microglia. We found that microglia upregulate TNFR2 mRNA and protein and shed large amounts of soluble TNFR2, but not TNFR1, in response to pro-inflammatory stimuli and through activation of TNFR2 itself. By microarray analysis, we demonstrate that TNFR2 stimulation in microglia regulates expression of genes involved in immune processes, including molecules with anti-inflammatory and neuroprotective function like granulocyte colony-stimulating factor, adrenomedullin and IL-10. In addition, we identify IFN-γ as a regulator of the balance between pro- and anti-inflammatory/neuroprotective factors induced by TNFR2 stimulation. These data indicate that, through TNFR2, microglia may contribute to the counter-regulatory response activated in neuropathological conditions.


Subject(s)
Inflammation/immunology , Microglia/metabolism , Receptors, Tumor Necrosis Factor, Type II/metabolism , Signal Transduction/physiology , Animals , Cells, Cultured , Gene Expression Regulation , Granulocyte Colony-Stimulating Factor/metabolism , Interferon-gamma/immunology , Interleukin-10/metabolism , Mice , Microarray Analysis , Microglia/cytology , Receptors, Tumor Necrosis Factor, Type I/genetics , Receptors, Tumor Necrosis Factor, Type I/metabolism , Receptors, Tumor Necrosis Factor, Type II/genetics , Tumor Necrosis Factor-alpha/metabolism
18.
Infect Immun ; 77(11): 4947-52, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19720761

ABSTRACT

Group I CD1 proteins are specialized antigen-presenting molecules that present both microbial and self lipid antigens to CD1-restricted alpha/beta T lymphocytes. The production of high levels of gamma interferon and lysis of infected macrophages by lipid-specific T lymphocytes are believed to play pivotal roles mainly in the defense against mycobacterial infections. We previously demonstrated that Mycobacterium tuberculosis and bacillus Calmette-Guérin (Mycobacterium bovis BCG) induce human monocytes to differentiate into CD1- dendritic cells (DC), which cannot present lipid antigens to specific T cells. Here, we show that in human monocytes mycobacteria trigger phosphorylation of p38 mitogen-activated protein kinase to inhibit CD1 expression in DC derived from infected monocytes. Pretreatment with a specific p38 inhibitor renders monocytes insensitive to mycobacterial subversion and allows them to differentiate into CD1+ DC, which are fully capable of presenting lipid antigens to specific T cells. We also report that one of the pathogen recognition receptors triggered by BCG to activate p38 is complement receptor 3 (CR3), as shown by reduced p38 phosphorylation and partial reestablishment of CD1 membrane expression obtained by CR3 blockade before infection. In conclusion, we propose that p38 signaling is a novel pathway exploited by mycobacteria to affect the expression of CD1 antigen-presenting cells and avoid immune recognition.


Subject(s)
Antigen Presentation/immunology , Antigens, CD1/biosynthesis , Dendritic Cells/microbiology , Monocytes/microbiology , Mycobacterium/metabolism , p38 Mitogen-Activated Protein Kinases/metabolism , Activating Transcription Factor 2/metabolism , Blotting, Western , Cell Differentiation/drug effects , Cell Differentiation/physiology , Dendritic Cells/immunology , Dendritic Cells/metabolism , Enzyme Inhibitors/pharmacology , Humans , Lipids/immunology , Macrophage-1 Antigen/metabolism , Monocytes/cytology , Monocytes/immunology , Mycobacterium/immunology , Phosphorylation , RNA, Messenger/analysis , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction/physiology
19.
Open Forum Infect Dis ; 6(1): ofy321, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30697571

ABSTRACT

BACKGROUND: Chikungunya virus is an emerging mosquito-borne pathogen with a wide global distribution. With the severe morbidity that it causes, chikungunya virus is a major public health problem in the affected areas and poses a considerable risk for unaffected areas hosting competent vector populations. In the summer of 2017, Italy experienced a chikungunya virus outbreak that spread in the Lazio region and caused a secondary outbreak in the Calabrian village of Guardavalle, with a final case number of 436. The causative strain was recognized as an Indian Ocean lineage (IOL) virus. METHODS: To understand the underlying genetic and molecular features of the outbreak virus, viruses from mosquito pools and clinical samples were isolated in cell culture and subjected to whole-genome sequencing and genetic analyses. RESULTS: All 8 characterized genomes shared a high sequence identity. A distinct substitution pattern in the Italian 2017 viruses (including mutations in E1, E2, and nsP4) was partly shared with the Pakistani 2016 outbreak viruses. Evolutionary analyses indicate that these 2 recent outbreaks and several geographically widely distributed, travel-associated viruses form a cluster of rapidly emerging Indian-origin IOL viruses. CONCLUSIONS: Our analyses show that the 2017 Italian outbreak virus belongs to a cluster of novel IOL chikungunya viruses originating in India. Their emergence calls for enhanced monitoring and strengthened preparedness measures, including vector control programs and raised awareness among general practitioners in countries potentially at risk.

20.
J Neuropathol Exp Neurol ; 67(5): 388-401, 2008 May.
Article in English | MEDLINE | ID: mdl-18431257

ABSTRACT

The roles of plasmacytoid dendritic cells (pDCs) and their response to interferon (IFN)-beta therapy in multiple sclerosis (MS) patients are poorly understood. We identified pDC accumulation in white matter lesions and leptomeninges of MS brains and abundant expression of the Type I IFN-induced protein MxA, mainly in perivascular CD3+ lymphocytes in lesions, indicating Type I IFN production by activated pDCs. The pDC chemoattractant chemerin was detected in intralesional cerebrovascular endothelial cells, and the chemerin receptor was expressed on infiltrating leukocytes, including pDCs. The effect of IFN-beta on pDC phenotype and function was evaluated in MS patients before and during IFN-beta treatment. Although IFN-beta did not modify the frequency and immature phenotype of circulating pDC, they showed lower expression of major histocompatibility complex Class II and blood-dendritic cell antigen 2 molecules and upregulation of CD38 and B7H1 costimulatory molecules. On exposure to CpG (a site where cytosine [C] lies next to guanine [G] in the DNA sequence [the p indicates that C and G are connected by a phosphodiester bond]) oligodeoxynucleotides in vitro, pDCs from IFN-beta-treated MS patients showed reduced expression of the pDC maturation markers CD83 and CD86 molecules; in vitro IFN-beta treatment of pDCs from healthy donors resulted in lower secretion of proinflammatory cytokines, including IFN-alpha, and a decreased ability to stimulate allogeneic T cells in response to maturative stimuli. These data indicate that IFN-beta modulates the immunologic functions of pDC, thus identifying pDCs as a novel target of IFN-beta therapy in MS patients.


Subject(s)
Cerebral Cortex/drug effects , Cerebral Cortex/immunology , Dendritic Cells/drug effects , Interferon-beta/pharmacology , Multiple Sclerosis/drug therapy , Multiple Sclerosis/immunology , Adult , Antigens, CD/analysis , Antigens, CD/metabolism , B7-H1 Antigen , Biomarkers/analysis , Biomarkers/metabolism , Cell Differentiation/drug effects , Cell Differentiation/immunology , Cerebral Cortex/physiopathology , Chemokines/drug effects , Chemokines/immunology , Chemotaxis, Leukocyte/drug effects , Chemotaxis, Leukocyte/immunology , Dendritic Cells/immunology , Female , GTP-Binding Proteins/drug effects , GTP-Binding Proteins/immunology , Humans , Immunologic Factors/pharmacology , Immunologic Factors/therapeutic use , Intercellular Signaling Peptides and Proteins , Interferon-beta/therapeutic use , Lymphocyte Activation/drug effects , Lymphocyte Activation/immunology , Lymphocytes/drug effects , Lymphocytes/immunology , Male , Middle Aged , Multiple Sclerosis/physiopathology , Myxovirus Resistance Proteins , Nerve Fibers, Myelinated/drug effects , Nerve Fibers, Myelinated/immunology , Nerve Fibers, Myelinated/ultrastructure , Phenotype , Plasma Cells/drug effects , Plasma Cells/immunology
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