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Viral Respiratory Infections in Patients with Cancer

AUTHORS

Yaser Arjeyni 1 , Hossein Goudarzi 2 , Gita Eslami 2 , Ebrahim Faghihloo 2 , *

1 Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran

2 Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran

How to Cite: Arjeyni Y, Goudarzi H, Eslami G, Faghihloo E. Viral Respiratory Infections in Patients with Cancer, Int J Cancer Manag. 2017 ; 10(2):e8084. doi: 10.5812/ijcp.8084.

ARTICLE INFORMATION

Iranian Journal of Cancer Prevention: 10 (2); e8084
Published Online: February 15, 2017
Article Type: Review Article
Received: August 31, 2016
Revised: October 24, 2016
Accepted: February 8, 2017
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Abstract

Context: Cancers are among the gravest causes of the intensive immunodeficiency and provide favorable conditions for severe respiratory tract infections.

Evidence Acquisition: Using various keywords related to the subject matter, articles were analyzed in PubMed and appropriately selected for review.

Results: In patients with cancer, some viral respiratory infections such as HRSV, Influenza virus, HCMV, HMPV and HPIV are prevalent.

Conclusions: Viral respiratory infections in cancer patients are common and can worsen the patients’ condition and disrupt the treatment process. Therefore, prevention and treatment of respiratory viral infections in cancer patients is important.

Keywords

Virus Respiratory Infection Cancer

Copyright © 2017, Iranian Journal of Cancer Prevention. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

1. Context

The accumulated evidence has supported involvement of viral respiratory infections in upper and lower respiratory tract illness around the world (1). In healthy persons, by the age of 2 - 60 years, these infections are usually suppressed by the host`s immune system, symptoms are limited to upper respiratory tract and infected individuals only experience slight and transient common cold-like symptoms (2). However, in children younger than 2 years, adults older than 65 years, patients with chronic lung disease, neuromuscular disease, airway anomalies, asthma or hemodynamically significant congenital heart disease and also in immunocompromised patients, the respiratory symptoms are more prevalent, severe and life-threatening (3-5). There are different agents causing immunodeficiency in human body. Among these, some types of cancers, especially hematological malignancies (e.g. chronic lymphoid leukemia and chronic myeloid leukemia) are among the important causes of the intensive immunodeficiency and provide favorable conditions for severe acute respiratory tract illnesses by directly affecting the immune system (6-10). This article reviews the importance of viral respiratory agents in some types of cancers.

2. Evidence Acquisition

In this review, decided decision has been made to take a glance at the prevalence of viral respiratory infections in cancer patients. Using keywords such as cancer, virus and respiratory infection, a PubMed search was conducted to find high quality articles pertaining to the central theme of this paper.

3. Results

3.1. Human Respiratory Syncytial Virus (HRSV)

Human respiratory syncytial virus (HRSV) is internationally classified as a member of pneumovirus genus from the subfamily of pneumovirinea and this subfamily is a subset of the virus family called paramixoviridea. This virus is divided into two major antigenic groups A and B on the basis of the G protein variability. The genome of the virus is a linear single stranded negative-sense RNA molecule containing 10 genes which encodes 11 proteins (2, 11, 12). M protein acts as a bridge between the envelope and ribonucleoprotein (RNP) of the virus and keeps these two parts tightly together, and cooperates in assembly and budding of the virion (12, 13). M protein also binds simultaneously to cellular actin (the main component of cell cytoskeletal microfilaments) and the viral RNPs, facilitating transport of these viral structures to the cellular plasma membrane location (14).

HRSV can cause upper and lower respiratory tract illness in all ages but the site of infection and severity of symptoms changes by the age and health status (4). HRSV is defined as the agent of childhood acute bronchiolitis and pneumonia around the world, with a frequency of 12% - 52%. Especially, in hospitalized children younger than 2 years, this frequency is estimated about 50% - 90% in acute bronchiolitis and 5% - 40% in pneumonia (15). 90% of children are infected with RSV during the first 2 years of life and up to 40% of them will develop acute lower respiratory tract infection (LRTI). In the United States, from 1980 to 1996, bronchiolitis, caused by RSV, was a common agent of hospitalization of infants less than one year of age, with the rate of more than 100,000 per year (16). In a study in 2005, the worldwide incidence of HRSV-associated ARTI in children younger than 5 years was evaluated about 33.8 million new episodes with at least 3 4 million episodes of LRTI necessitating hospital admission. About 66,000 to 199,000 children younger than 5 years died of HRSV associated acute lower respiratory tract infection in 2005, of which 99% occurred in developing countries (17). In Iran, HRSV is responsible for 20% acute respiratory infection in younger children (18-20). Infection by this virus is considered as one of the most important causes of seasonal respiratory complications in adults (2). 25% of mortality attributed to respiratory infections in cold seasons is due to HRSV, which in this respect is like influenza virus. Approximately 80% of mortalities caused by respiratory infection of HRSV occur in the elderly. General symptoms include fever, headache, myalgia, sneezing, sore throat, dry cough, rhinorrhea, bronchitis and otalgia, but the infection can spread to the lower respiratory tract of the risk groups mentioned above, which subsequently leads to wheezing, tracheobronchitis, severe bronchiolitis and pneumonia (2).

HRSV infection can cause considerable morbidity and mortality in leukemia patients. However, treatment with aerosolized ribavirin may prevent spreading of infection to the lower respiratory tracts and developing pneumonia in patients at the stage of upper respiratory tract infection (URTI).

Torres et al worked on outcomes of HRSV infection in leukemia patients. 52 patients with the median age of 47 years (range from 1-83 years) were evaluated, from which 34 patients (65%) were male and 34 patients (65%) had acute leukemia. 46 patients were admitted to the hospital of which 27 (52%) developed pneumonia secondary to HRSV. 5 (19%) out of the 27 cases died because of pneumonia. There was a trend toward a higher rate of progression from URTI to pneumonia in males compared to females (74% vs 56%). Viral and bacterial co-infections were diagnosed in nine (17%) of all patients five of which involved the lung (21). In a study performed between 2004 and 2009 on the molecular epidemiology of HRSV subgroups A and B in Irish adults with hematological malignancy, a total of 980 samples were evaluated for infection by this virus via immunofluorescence, from which 60 evaluable samples were HRSV-positive. The patients had various blood malignancies covering chronic myeloid leukemia (10 cases), chronic lymphocytic leukemia (10 cases), acute lymphoblastic leukemia (10 cases), acute myeloid leukemia (9 cases), non-Hodgkin`s lymphoma (8 cases), multiple myeloma (7 cases), mantle cell lymphoma (2 cases), and aplastic anemia (2 cases). Nearly 50% (n = 31) of these patients were hospitalized for treatment with aerosolized ribavirin because of severe complications of HRSV infection. The A subgroup frequency was 52% versus 48% for subgroup B. Among the eight genotypes of HRSV A, two of them GA2 and GA5 were observed in this study. The only identified genotype from subgroup B was the BA genotype (22).

In 1997, Mazzulli et al. performed a molecular characterization study on a nosocomial outbreak of HRSV in an adult leukemia-lymphoma ward in the PMH cancer hospital. BAL samples were collected from 45 patients and then cultured on rhesus monkey kidney (RMK), MRC-5 and HEp-2 cell lines. Six cultures were positive for HRSV of which 5 cultures also had positive results by direct immunofluorescence staining. Then RT-PCR was performed on BAL specimens and RNAs extracted from the HRSV positive cultures. Test results were positive for 5 of the 6 cultures and also for two additional BAL specimens. After sequencing six GB3 and one GA5, genotypes were discovered by genotyping. Four patients died 23 - 64 days after onset of respiratory symptoms (23).

Moreira et al performed an epidemiological and methodological study of HRSV detection among children and patients with hematological malignancies receiving hematopoietic stem cell transplant (HSCT). In this study, 102 samples were collected from 67 HSCT recipients among whom there were 19 (28.8%) leukemia cases, 22 (33.3%) lymphoma cases and 25 (37.9%) cases with other hematological malignancies who had 4 (22.2%), 7 (38.9%) and 7 (38.9%) positive HRSV samples respectively (Table 1). Two separate episodes of HRSV occurred in one of these patients in 2008 (24). From January 16 to February 4, 2004, 6 RSV infected patients with hematological malignancies were admitted to an adult HSCT unit with the ages of 41, 26, 61, 62, 61 and 67 years who had cutaneous T cell lymphoma, nodular sclerosing Hodgkin disease, multiple myeloma, CML, mantle cell lymphoma and CML respectively, from which the second and the last (33%) developed URTI and other four patients (67%) developed HRSV-associated pneumonia. Two of these cases died due to the pneumonia (25).

Table 1. Studies Worked on Frequency and Outcomes of Viral Respiratory Infections in Cancer Patients
AuthorsDatePatientsDiagnostic Method(s)Detected VirusesURTILRTIPneumoniaaViralb
RSVFlu AFlu BHCMVHPIVHMPVAdenoPicornaCoronaNo (%)CauseNo (%)CauseNo (%)CauseNo (%)Cause
Torres et al.200752-52--------46 (88)RSV27 (52)RSV27 (52)RSV5 (19)Pneumonia
Salter et al.2004 - 2009980IF60 (60)--------31 (52)RSV31 (52)RSVNDNDNDND
Mazzulli et al.199945IF Cell culture RT-PCR6 (13)--------NDNDNDNDNDND4 (9)ND
Moreira et al.201367ND18 (27)--------NDNDNDNDNDNDNDND
Kassis et al.20106-6--------2 (33)RSV4 (67)RSV4 (67)RSV2 (33)Pneumonia
Small et al.2002548DFA EIA Cell culture48 (9)--------NDND25 (4.6)RSV25 (4.6)RSV3 (0.5)Pneumonia
Ghosh et al.1992 - 2000249ELISA IF Cell culture9 (4)--------NDNDNDND6 (2.4)RSV2 (0.8)Pneumonia
Anaissie et al.1997 - 1998190IF Cell culture56 (29)--------NDNDNDND6 (11)RSV3 (5)Pneumonia
Roghmann et al.200362Cell culture RT-PCR9 (15)13-5--3-18 (29)RSV Flu B HPIV3 Flu A picorna3 (5); 2 (3)RSV; Flu BNDNDNDND
Benites et al.2014104Rapid test real-time -PCR9 (9)33-13-247NDNDNDNDNDNDNDND
Souza et al.44IF real-time -PCR-24-------NDND10 (41)Flu ANDND5 (21)Respiratory failure
Rodrigues et al.20128CT-scan-8-------NDNDNDND5Flu A2Refractory hypoxia
Tasian et al.200825DFA Cell culture real-time -PCR-204------NDND16Flu3FluNDND
Pollara et al.201376Multiplex real time RT-PCR23 (30)--------NDND3 (4)Flu A3 (4)Flu A3 (4)Pneumonia
Redelman –Sidi et al.2010394DFA; Cell culture; real-time PCR-45-------NDND6Flu ANDNDNDND
Gonzalez et al.1999204IF; Cell culture-8--2-39-
5Flu7Flu A7Flu A4Pneumonia
6Picorna6Picorna6Picorna5Pneumonia
2Adeno3Adeno3Adeno5Pneumonia
2HPIV1HPIV1HPIV2Pneumonia
Porter et al.1999118Cell culture; IE; staining25111----NDND
4Flu A4Flu A2Pneumonia
1Flu B1Flu B1Flu B
2RSV2RSV1RSV
1HPIV; HCMV1HPIV; HCMV1HPIV
Jojima et al.200158PCR---5-----NDND5 (9)HCMV5 (9)HCMV6 (10)Pneumonia
Chang et al.201117Pathology, IF, EIA, shell vial culture---10-----NDNDNDND7 (41)HCMV2 (12)HCMV
Maeng et al.20121554DFA; Rapid test; Cell culture----74----59HPIV15HPIV12HCMV5ARDS and Pulmonary Hemorrhage
Srinivasan et al.2011820DFA; Cell culture; Real-time PCR----83----66HPIV17HPIVNDNDNDND
Chemaly et al.2012200-----200----140HPIVNDND60HPIV16Pneumonia
Williams et al.2005128DFA; Cell culture; RT-PCR1120--62252-20HMPV9HMPV9HMPV3Pneumonia
Kamboj et al.20082125DFA;Real-time PCR1----51---NDNDNDNDNDND1RSV

aPneumonia and other clinical lung diseases.

bDeaths attributable to viral infection.

In another study (Small et al. 1994 - 2001), 548 patients, who had received HSCT, were evaluated for HRSV infection. Among them 48 allogeneic HSCT patients had a positive result for HRSV infection by direct fluorescent antibody test (DFA), enzyme immunoassay (EIA) and Conventional cultures in rhesus monkey kidney cells, of whom 37 patients had hematological malignancies including CML and CLL (11 cases), acute leukemia (22 cases), lymphoma (3 cases) and multiple myeloma (1 case). In this study, twenty-five HRSV infected patients developed lower respiratory tract disease (LRTD) and pneumonia. Sixteen of them had hematological malignancies. Three patients died due to pneumonia (26). During eight consecutive winters 1992 - 2000, HRSV infection was investigated in 249 hospitalized women with breast cancer who had received autologous blood and marrow transplant. By means of ELISA, indirect immunofluorescence and cell cultures (Madin–Darby canine kidney cells, rhesus monkey kidney continuous cell line (LLC-MK2), human laryngeal tumor cells (Hep-2) and human embryonic lung fibroblasts (WI-38)), HRSV infection was detected in nine patients. Six of these patients developed pneumonia and two of them died due to the pneumonia (27).

The natural history of HRSV infection in cancer and transplant patients was studied by Anaissie et al from October 3, 1997 to October 14, 1998. Nasopharyngeal wash, BAL and lung biopsy samples were collected from 190 cancer patients with the median age of 58 years, prior to chemotherapy. 147 (77%) patients were considered as multiple myeloma (MM). Samples were cultured in tubes containing human diploid embryonic lung (MRC-5) fibroblast cells and were checked daily for the characteristic RSV cytopathic effect (CPE). Cultures with CPE were considered HRSV positive if they were confirmed by an indirect immunofluorescence test. Samples which had a negative culture but a positive IFA result also considered as positive. HRSV infection was totally positive in 56 of 147 MM patients of whom 6 (11%) developed pneumonia, 5 (9%) were transferred to intensive care unit (ICU) and 3 (5%) died within 30 days of therapy (28).

Other studies also have reported high incidence of HRSV in a variety of age groups. Roghmann et al. investigated respiratory viral infections (RVI) in 62 outpatient adults who had undergone SCT. 37 episodes of respiratory symptoms were observed in 35 (56%) patients. Nasopharyngeal aspirates were taken from each episode at the onset of respiratory symptoms and were subsequently tested for respiratory viruses using culture and RT-PCR. Viral respiratory tract infections were confirmed in 22 episodes. RSV was discovered in 9 episodes 6 of which developed URI and 3 remaining episodes led to LRI. Other viruses included Flu B, HPIV3, Flu A and picornavirus which resulted in 3, 5, 1 and 3 episodes, respectively. All of these episodes led to URI and just Flu B virus caused 2 LRI cases (29).

In another investigation by Benites et al. on acute RVI in pediatric cancer patients receiving chemotherapy, 104 children under 21 years of age suffering from different malignancies with dominancy of ALL and osteosarcoma were examined for acute RVI. Collected nasopharyngeal aspirates were tested for RVI by rapid test (for influenza virus) and multiplex real-time PCR. Results showed that rhinovirus, RSV A and B, HMPV A and B, influenza B, coronavirus 229, coronavirus 43, influenza A, coronavirus 63, parainfluenza and influenza A/H1N1 were responsible for acute RVI (30). Clinical outcomes of HRSV infection also were studied among immunocompromised outpatient children with hematologic malignancy, solid organ transplant or hematopoietic cell transplant. The majority of HRSV infections (n = 37, 69%) were identified in hematologic malignant cases among which 16, 27, 24 and 2 cases showed fever, cough, rhinorrhea and wheezing, respectively which were higher compared to transplant recipients. Also one hematologic malignant patient was admitted to ICU due to HRSV infection (31).

3.2. Influenza Virus

Influenza viruses are respiratory pathogens from the family of orthomixoviridea and genus Orthomyxovirus which are categorized into types A, B and C based on the variation in their nucleoprotein (NP) and M1 antigens (32, 33). Influenza viruses have a segmented negative-sense single stranded RNA genome (34). In Influenza A and B viruses, the genome contains eight segments of ssRNA but influenza C virus contains only seven segments of ssRNA (35, 36).

Influenza symptoms usually appear 1 to 3 days after being infected and often include: fever, dry cough, tiredness/extreme exhaustion, dyspnea, wheezing, headache, muscle and joint pain, sore throat and stuffy nose (37-39). Most people recover within a week but cough and tiredness may persist. Infected persons can disperse influenza to others one day before they become sick and 5 - 10 days after they become sick for adults and even longer for young children (40, 41). Influenza can escape from the human immune response due to rapid antigenic shift and drift (42). Because of this transient immunity, influenza can persist in small populations and sicken persons in all ages especially children younger than 2 years, adults older than 60 years, immunocompromised patients and pregnant women in whom the disease is more severe and fatal, and can develop severe pneumonia (43-46). Due to several genome rearrangements happening among influenza subtypes, infection by this virus has led to four pervasive pandemics (1918-1919 A(H1N1)–1957 A(H2N2)-1968 A(H3N2)- 2009 A(H1N1)) (47-50).

In a cohort study by L. Souza et al, the pandemic H1N1 influenza A infection (2009) was investigated in 44 hospitalized cancer patients (median age 14.5, range 3 - 69 years) all of whom had an influenza-like illness. After screening by indirect immunofluorescence and real-time RT-PCR, influenza infection was confirmed in 24 patients. Hematologic malignancy was observed in 18 (75%) of these patients, whereas solid tumors were observed in 6 (25%) patients. 13 (54%) patients were transferred to intensive care unit (ICU). 10 (41.6%) needed mechanical ventilation. The overall mortality in this study was about 21% (n = 5) (51). A group of scientists surveyed chest computed tomography (CT) scans in 8 influenza infected neutropenic cancer patients with fever and severe pneumonia. Respiratory failure was diagnosed in six (75%) of these patients and all of them were transferred to the intensive care unit (ICU). Four patients required invasive mechanical ventilation. From all patients, five developed pneumonia, two had CT scans indicating bronchitis and bronchiolitis, and others had signs of chronicity. Two patients died due to refractory hypoxia secondary to pulmonary alveolar hemorrhage and acute respiratory distress syndrome (ARDS) (52).

Tasian et al. performed a study on morbidity of influenza infection in children with cancer. The patients had various cancer types including acute lymphoblastic leukemia (10 patients), acute myelogenous leukemia (1 patient), Hodgkin lymphoma (1 patient), non-Hodgkin lymphoma (1 patient), Langerhans cell histiocytosis (2 patients), Wilms tumor (2 patients), osteosarcoma (2 patient), rhabdomyosarcoma (2 patients), neuroblastoma (3 patients), and brainstem glioma (1 patient). About 63% of these patients had lymphopenia. The infection was detected in Nasal wash specimens, BAL fluid, endotracheal tube aspirations, lung biopsies, and nasal swabs using direct fluorescent antibody (DFA) testing, viral culture and real time RT-PCR. Twenty-four influenza infected pediatric cancer patients (20 influenza A and 4 influenza B cases) with 27 clinical encounters were diagnosed. Two-thirds of patients were hospitalized due to severe respiratory symptoms. Primary influenza pneumonia occurred in three children. Mechanical ventilation was needed for 4 (15%) clinical encounters. Six patients had oxygen requirement for up to 30 days. No patients died during this study (53). In January 2011, a nosocomial outbreak of pandemic influenza A (H1N1pdm09) in hematologic patients was investigated for detection of oseltamivir resistant (OST-r) variants. 134 nasopharyngeal swabs, bronchoalveolar washes or respiratory secretions were collected from 76 hospitalized patients (age range: 23 - 76 years) and multiplex real time RT-PCR was done for matrix gene in order to distinguish influenzas A and B. Then influenza A positive samples were searched for H1N1pdm09 subtype using a fast real time PCR system and at last oseltamivir resistant variants were determined by means of RT-PCR and Sanger sequencing. Totally, 23 (30.2%) out of 76 patients were positive for H1N1pdm09 infection. Six of these patients with ages 76, 50, 39, 42, 65 and 24 years were suffering from Non Hodgkin lymphoma, diffuse large cell Lymphoma, non Hodgkin lymphoma, acute myeloid leukemia, multiple myeloma and acute lymphoblastic leukemia respectively. Three of them developed acute respiratory distress syndrome and required intubation and mechanical ventilation, and eventually died because of fatal influenza pneumonia. Three patients were infected by OST-r variant (54). Redelman-Sidi et al. investigated this infection in cancer patients and hematopoietic stem cell transplant recipients. Nasopharyngeal swabs taken from 394 patients (age range of 3 - 80 years) were analyzed using DFA, culture in RMK cells and real time RT-PCR (for detection of viral load). The H1N1pdm09 was detected in 45 (11%) of these patients. 96 of 394 patients were HSCT recipients among whom 43 were with hematologic cancers and 16 were with solid tumors. 22% (n = 21) of the HSCT recipients were positive for H1N1pdm09 6 of whom developed LRTI. One patient with multiple myeloma was transferred to intensive care unit. No deaths occurred due to influenza infection (55). In a study GONZALEZ et al. searched for community respiratory virus infections (CRVI) in 224 BAL samples taken from 204 hematological malignant patients. CRVIs were detected in 21 cancer patients including 4 AML, 7 ALL, 6 non-Hodgkin’s lymphoma, 2 Hodgkin’s disease, 1 CLL and 1 neuroblastoma cases using culture in human fibroblasts (MRC5), human epithelial cells (Hep-2 and A-549) and Madin-Darby canine kidney cells (MDCK) cell lines and then were confirmed by immunofluorescence. Experiment results specified 8, 8, 3, 2 and 1 episodes of respiratory infections caused by influenza A virus, enterovirus, adenovirus, parainfluenza virus and rhinovirus, respectively. 15 cases of URTI occurred of which 5 were due to influenza, 5 were due to enterovirus, 2 were due to adenovirus, 2 were due to PIV and 1 was due to rhinovirus. Influenza A infection caused pneumonia in 7 patients and 4 of those led to death. Other 3 viruses, namely enterovirus, adenovirus and parainfluenza virus, were known as the cause of 6, 3 and 1 pneumonia cases respectively. Five patients died due to enteroviral pneumonia and two died because adenoviral pneumonia. No pneumonia or deaths were reported following rhinovirus infection (56).

Porter et al, reported several cases of RVI in 118 cancer patients (54 leukemia or lymphoma, 46 carcinoma and 18 sarcoma) who were died with malignant tumors. Autopsies taken from respiratory tract of all cases were examined by cell culture and Immunoenzyme staining. Viral antigens were found in 8 of all samples of which 5 were influenza A, one was influenza B, 2 were RSV and one was coinfected by HPIV1 and CMV. Diffuse alveolar damage was observed in one influenza A case, one influenza B case, two RSV cases and the last coinfected case. Clinical lung disease also was confirmed in all cases but one influenza case. Two deaths were due to diffuse alveolar damage and Pneumonia caused by influenza A. Respiratory failure by each of other detected viruses led to one death (57). In an epidemiology study of viral pneumonia in 38.5 - 70.5 year old adults, etiologic agents of pneumonia were identified by using FilmArray respiratory panel assay. Of the 284 adults with proven viral pneumonia, 95 (33.5%) had an active malignancy and the most frequent viral etiologies were influenza (24.3%), rhinovirus or enterovirus (23.6%), PIV (13%), and RSV (10.6%) (Table 1). The majority of patients with multiple viral infections had active malignancy. Fifty-eight of malignant patients were admitted to ICU following viral pneumonia (58). In another study, frequency of respiratory viral infections among children suffering from febrile neutropenia caused by cancer chemotherapy was surveyed by in-house real-time PCR. The most frequent viral infections were covering rhinovirus (n = 21, 24%), human Coronavirus (n = 7, 8%), influenza (n = 4, 5%), HRSV (n = 3, 3%), HPIV (n = 3, 3%), and HMPV (n = 2, 2%) (59).

3.3. Human Cytomegalovirus (HCMV)

Cytomegalovirus infection is known as an important cause of mental retardation in children and multi organ failure and lethal systemic infection among immunocompromised patients (60-63). CMV is classically located in cytomegalovirus genus from betaherpesvirinea subfamily of herpesviridea family. This virus is also known as human herpes virus 5 (HHV-5). The viral genome is a double stranded linear DNA which is encapsidated in an icosahedral capsid and a lipid bilayer envelope containing viral surface glycoproteins has covered this nucleocapside. (64). The viral capsid proteins include MCP, CAP, TRI2, and SCP. Major tegument proteins consist of pp65, RR1, pp150, LTP, pp71 and VPK. The most important envelope glycoprotein is gB protein which mediates attachment to heparin sulfate and assists with gH and gL proteins in fusion with host cell membrane (65-73).

CMV infection should be considered as a causative agent of pneumonia in non-transplanted cancer patients, particularly if steroids are a component of their therapy. A study was performed on diagnosis and treatment of pulmonary opportunistic infections (Pneumocystis carini and CMV) in hematological malignant patients. These infections were discovered in sputum and lung biopsy samples collected from a total of 58 malignant patients by PCR, of which 7 (12.1%) cases were positive for Pc and 5 (8.6%) for CMV all of whom developed pneumonia. Totally 12 patients died because of respiratory failure. 6 of these were due to CMV (4 cases) and mucor pneumonia (2 cases), and the remaining 6 deaths were due to underlying malignant diseases. In 7 PCR positive Pc infected patients, early treatment was effective in all of them and the deaths occurred following this infection were due to pathologic effects of CMV and mucor mycosis (one case with CMV only and one case with CMV and mucor coinfection). For CMV despite antiviral therapy, 3 of 5 PCR positive patients died from pneumonia. In addition, the level of fungal β-glocan in blood indicated mycotic pneumonia in nine of all patients and the treatment was effective in 7 of them (74). Chang et al. reported a case series of CMV infection in non-transplant patients (age range: 29 - 86) with hematologic malignancies. Serum and biopsy samples were collected from these patients. Then using clinical symptoms, radiographic results and laboratory tests, 20 episodes of infection were examined in 17 patients overtaken blood malignancies. Laboratory methods included histopathology, immunofluorescence, enzyme immunoassay and shell vial culture, which were used for detection of CMV inclusion bodies, pp65 antigens, CMV specific IgM or IgG in serum and shedding in BAL fluid, respectively. CMV infection occurred in 12 of 20 episodes. 10 patients had a positive CMV antigen assay. 7 patients developed pneumonia caused by CMV-D subtype and also their BAL samples resulted in positive culture. Among 17 patients, 6 survived within a 4 - 14 month follow up, one patient lost to follow up, and the remaining 10 patients died within a < 1 - 27 month period when CMV-D was the causative agent of two deaths. One death was due to CMV pneumonia (75).

3.4. Human Metapneumovirus (HMPV)

A considerable part of lower respiratory tract failures caused by viruses can be attributed to human metapneumovirus (HMPV). This virus is a member of metapneumovirus genus from pneumovirinea subfamily from paramixoviridea family and this family is a subset of the mononegavirals order. HMPV is a pleomorphic virus which is 150 - 600 nm in diameter. HMPV, like other members of paramixoviridea, contains a single stranded negative-sense RNA molecule. The gene order of virus (from 3’ to 5’) is N(nucleoprotein)- P(phosphoprotein)- M (matrix protein)- F (fusion protein)- M2(cods for M2-1 and M2-2)- SH(small hydrophobic protein)- G(attachment protein)- L(viral polymerase) (76-78).

Seroprevalence of HMPV among children with the age of 5 years is almost 100%. In a study by Walsh et al, the proportion of HMPV infection was between 3% - 7.1% in adult individuals (79). In this study HMPV infection was associated with hospitalization because of acute RTI and the incidence of infection in the hospitalized patients was 4.3% - 13.2% (80). In another study by widmer et al. the rate of hospitalization due to HMPV acute RTI was 4.5%. From the clinical aspect, most patients admitted with cough, nasal congestion and dyspnea. More severe symptoms include purulent cough, wheezing, fever, sore throat, bronchitis, bronchiolitis, pneumonia, conjunctivitis and otitis media (81).

HMPV has been reported as a prevalent cause of respiratory failure among cancer patients. Williams et al. (1999 - 2004) compared this infection with other respiratory viral infections in adults with hematological malignancy (age range: 20 - 72). Nasopharyngeal aspirations and BAL samples from 251 episodes of respiratory infection in 128 malignant patients were surveyed for viral etiologies using direct immunofluorescence assays (DFA), cultureed in LLC-MK2 cells and RT-PCR. Among 22 patients who tested positive for HMPV, 20 had URTI, 9 developed LRTI as pneumonia which led to 3 deaths. The number of pneumonia caused by other detected infections including influenza, RSV, PIV1&3, adenovirus, rhinovirus and enterovirus was 20, 11, 6, 5, 0 and 2 cases and the number of deaths which occurred due to the first four infections was 4, 3, 2 and 2 cases and no deaths were associated with latter two infections (82). In another study, data acquired from analyzing 2795 nasopharyngeal swabs and bronchoscopy specimens of 2125 patients with solid tumors, leukemia, lymphoma and other hematological disorders were investigated for HMPV infection. Applied laboratory methods included DFA and real-time PCR. HMPV infection was diagnosed in 51 patients. No severe respiratory symptoms were caused by HMPV but one patient died due to coinfection with RSV and toxoplasma (83).

3.5. Human Parainfluenza Virus (HPIV)

Human parainfluenza virus (HPIV) is a prevalent cause of upper and lower respiratory failure chiefly in infants and young children (84). There were more than 5 million LRI cases each year during 1980 - 86 in the United States in children younger than 5 years. HPIVs 1 - 3 had been identified in about one-third of these infections (85-87). Most children with the age of 6 - 10 years have evidence of past infection (92). 3% - 18% of all admissions to pediatric hospitals are due to acute respiratory infections (ARTI) and HPIV infection was detected in 9% - 30% of these patients (87-89). LRI causes 25 to 30% of deaths in childhood and HPIV causes at least 10% of these LRIs. Mortality caused by HPIV often is seen in young infants, immunocompromised patients and the elderly (1).

In a study by lewis et al. (1991 - 1994) the rates of developing parainfluenza pneumonia and mortality among bone marrow transplant (BMT) recipients were 44% and 37%, respectively (90). HPIV infection usually causes otitis media, pharyngitis, conjunctivitis, and coryza. More severe symptoms include croup (acute laryngotracheobronchitis), Tracheobronchitis, Bronchiolitis, pneumonia and Neurologic diseases (89, 91-94).

In terms of classification, this virus is a member of mononegavirals order, paramixoviridea family and subfamily of paramixovirinea. Four types (1, 2, 3 and 4) are determined for HPIV. The type 4 is subdivided to 4A and 4B subtypes. The types 1 and 3 fall into respirovirus genus but types 2 and 4 are categorized in rubulavirus genus. This virus is a pleomorphic virus that is 150 - 250 nm in diameter with a lipid envelope covering helical nucleocapside (91-94).

In a retrospective study, the data recorded between January 2000 and July 2008 from 1554 pediatric cancer patients were examined for consequences of HPIV infection. BAL and tracheal aspiration samples were taken from the patients and then tested by direct fluorescent antibody assay DFA, rapid antigen tests and cell culture method. 137 (6.4%) of all patients were overtaken a viral respiratory infection who 74 (54%) of them were infected by HPIV. HPIV3 was the dominant subtype among the patients. 59 (79.7%) of HPIV infected children had upper respiratory tract infection (URTI) while 15 (20.3%) of them had lower respiratory tract infection (LRTI). 12 of URTI cases had developed pneumonia subsequently. 59 of HPIV infections were nosocomial cases. 5 of 27 LRTI cases finally died due to respiratory failure (4 due to ARDS and one due to pulmonary hemorrhage) (95).

Srinivasan et al. (2000 - 2009) performed another retrospective study on HPIV infection in 820 hematological malignant children. Nasopharyngeal swab and wash samples were taken from patients. By infection of rhesus monkey kidney, A549 and MDCK cell lines and using DFA staining and real-time PCR, HPIV infection was confirmed in 83 (10%) of all patients the majority of whom were < 2 years old and suffering from ALL. HPIV1-4 subtypes also were distinguished on the basis of hemadsorption outcomes. URTI was diagnosed in 66 (80%) of infected patients and the remaining 17 patients developed LRTI. Despite mechanical ventilation requirement in 3 children, none of them died due to respiratory failure (96). Chemaly et al. in their research diagnosed HPIV infection in 200 patients including 80 leukemia cases and 120 hematopoietic stem cell transplant (HSCT) recipients. Most frequent malignancies were Acute myeloid leukemia (44%) and acute lymphoblastic leukemia (28%). 70% of patients had URTI and the remaining 30% had developed pneumonia at the time of admission. Among leukemia patients, 10 were transferred to ICU due to severe pneumonia and 8 of them needed mechanical ventilation all of whom died of respiratory failure. For HSCT recipients, the rates of transmission to ICU, mechanical ventilation requirement and death due to pneumonia were 7, 5 and 8 cases, respectively (97).

4. Conclusions

In summary, viral respiratory infection is caused by HRSV, influenza virus, HCMV, HMPV and HPIV is prevalent in patients with cancer. These infections can worsen the patient's condition and disrupt the treatment process. On the other hand, viral respiratory infection easily spread in the hospital parts and control of these infections is difficult. Therefore, prevention and treatment of respiratory viral infections in cancer patients is of great importance.

Acknowledgements

Footnotes

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