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SM Vaccines and Vaccination Journal

Factors Associated with Human Papilloma virus Vaccination among White-American Females

Abstract Citation Introduction Materials and Methods Results Discussion Strength Limitations Conclusion Acknowledgment References
Details

Received: 07-Jun-2018

Accepted: 05-Jul-2018

Published: 10-Jul-2018

Jyothi Sagar Guddappa, Shayesteh Jahanfar*, Joseph Inungu and Neli Ragina

Master of Public Health Program, School of Health Sciences, Central Michigan University, USA

Corresponding Author:

Shayesteh Jahanfar, Master of Public

Health Program, School of Health

Sciences, Central Michigan University,

Mount Pleasant, Michigan, USA,

Keywords

HPV Vaccination; Cervical Cancer; Health Care; Health Insurance; White-American females

Abstract

Introduction: Human papilloma virus (HPV) is a public health concern because of its association with cervical cancer. Despite the evidence about HPV vaccination benefits, debate persists about the rate of receiving HPV vaccination.

Objective: The main objective of this study is to examine the uptake rate of HPV vaccination among White-American females.

Design and Method: This study analyzed data from the 2015 and 2016 National Health Interview Survey (NHIS), a cross sectional study of non-institutionalized population in the United States. Females aged 18-85 years were included in the survey.

Result: The White-American females odds are (OR=3.84; 95% CI 2.74-5.39) three times higher than males.

Conclusion: Our results highlight the uptake rate of HPV vaccination in preventing cervical cancer among White-American population.

Citation

Guddappa JS, Jahanfar S, Inungu J and Ragina N. Factors Associated with Human Papilloma virus Vaccination among White-American Females. SM Vaccine Vaccin. 2018; 4(1): 1021.

Introduction

Cervical cancer is an important public health problem in the United States1. It is caused by Human Papilloma Virus (HPV). About 20 million people have genital HPV and 6.2 million people are infected annually in the United States [1]. Approximately, 50% of HPV infections spread through skin-to-skin and oral contact during sexual activity [2]. HPV is one of the most common sexually transmitted infections with the potential to cause genital warts, warts in the throat, and cancers of the vulva, vagina, penis, anus, mouth, and pharynx [4]. The incidence and mortality rate of cervical cancer due to HPV infection are higher among White-Americans and African-Americans compared to Latin-American women living in low socioeconomic areas [5].

In addition, the prevalence of HPV among females aged 15-19 and 20-24 are estimated to be 33% and 54%, respectively [6]. About 87% of all HPV cases are females [6]. In particular two HPV types (16 and 18) cause approximately 70% of cervical cancers, whereas two other types (6 and 11) cause approximately 90% of anogenital warts [7,8]. The HPV vaccine was approved by Food and Drug Administration (FDA) in 2006 for females [9]. Currently in the United States, there are two types of HPV vaccines available: bivalent and quadrivalent vaccines [6]. Both vaccines protect against the two HPV types causing 70% of cervical cancer [6]. These two vaccines are Gardasil and Cervarix (HPV4 Gardasil approved in 2006 and Cervarix approved in 2009) [10]. These two vaccines have demonstrated safety and nearly 100% efficiency in protecting against HPV 16 and HPV 18 responsible for genital warts and warts in the respiratory tract [1]. The vaccine should be administered to 13-26 year old girls before the onset of sexual activity [1]. These vaccine are administered as a 3-dose series with the 2nd and 3rd dose given at 2 and 6 months following the first dose [6,7]. The HPV vaccine was proven as an effective preventive measure to reduce the public health burden of cervical cancer and HPV related diseases [7].

In the literature, there are many factors associated with the HPV vaccination. The factors that were consistently shown to be positively associated with HPV vaccination are: higher maternal education, more access to health care, and health insurance coverage. Furthermore, other factors include access to health care, knowledge about HPV infections, as well as vaccine acceptability, reasonable cost of the vaccine, higher perceived effectiveness of the vaccine, and less fear of side effects of the HPV vaccine such as fever, headache, dizziness, nausea, vomiting, diarrhea, insomnia, sore throat, cough, tooth pain, and muscle pain [5-7].

This study aims to examine the uptake rate of the HPV vaccination among White- American females. The study also analyzes other factors related to the HPV vaccine such as, health care changes in the past 12 months, changes related to health insurance, and uptake of other vaccines including hepatitis A & B.

Materials and Methods

Data

Data from the 2015 and 2016 National Health Interview Survey (NHIS) were analyzed. The NHIS is a cross-sectional household interview survey. Samples were collected by conducting continuous quarterly (1-4) interviews throughout each year [12]. The household interview surveys population with age-range between 18-85 years old. The total NHIS sample is subdivided into four separate panels, or sub designs, such that each panel is a representative sample of the U.S. population. The main objective of the NHIS is to monitor the health of the United States population through the collection and analysis of data on a broad range of health topics. A major strength of this survey lies in the ability to display these health characteristics by many demographic and socioeconomic characteristics. The NHIS covers the civilian noninstitutionalized population residing in the United States at the time of the interview [12]. Data is collected through a personal household interview conducted by interviewers employed and trained by the U.S. Census Bureau [12]. Approximately, 1-2 participants are randomly selected per family. These individuals must self-report responses to questions in this section. The NHIS questionnaire uses a Computer Assisted Personal Interviewing (CAPI) mode. The CAPI version of the NHIS questionnaire is administered using a laptop and interviewers enter responses directly into the laptop during the interview. This computerized mode offers distinct advantages in terms of timeliness of the data and improved data quality [12].

Study variables

Independent variables: The independent variables consisted of the following socio-demographic personal characteristics: age (18 85 years), sex (male and female), marital status (married, others [widowed, divorced, separated]), region (Northeast, Midwest, South, and West), race/ethnicity (white-American, African-American, American-Indian, Alaska-Native, Asian, and Multiple race including (Chinese, Filipino, other Asian), changes of health insurance plans (yes/no), and changes of healthcare place in the past 12 months (yes/ no). Were hepatitis A & B vaccines received? What was the number of hepatitis A vaccine received? Pap-smear test done in the past 12 months?

Dependent variables: The self-reported HPV vaccination was our outcome of interest. Participants in the 2015& 2016 NHIS survey were asked, “Have you ever received HPV shot/vaccination?” (The variable coded as 1=Yes and 2=No).

Statistical analysis

Descriptive statistics summarized the characteristics of the sample. Inferential statistics included in Chi-square test to identify association between two categorical variables. We then conducted univariate and multivariate logistic regression model of analysis including variables that were found to be significantly associated with dependent variable. Results of the logistic regression were presented as the odds ratio (OR) and associated 95% confidence interval (95% CI). All statistical analyses were performed using IBM SPSS statistics for windows, version 24 (IBM Corp. Released 2015. IBM SPSS Statistics for Windows, Version 24.0. Armonk, N. Y: IBM Corp).

Results

The sociodemographic characteristics of the participants in the 2015 & 2016 NHIS are summarized in the Table 1. Total (n=66,700) female and male participants in this study. About 54.9% of the participants were female (n=36,638). The majority of participants were married (42.5%), females (54.9%), White-American (78.5%) and resided in the South region (34.7%), with average age (50.35±18.49 SD) that ranged from 18-85 years. Among the 66,700 respondents, 3,999 (6%) reported ever receiving HPV vaccination. With regard to other preventive measures, 26.5% of respondents reported receiving hepatitis B vaccine, 13.1% received hepatitis A, and 23% had a Pap smear test during past 12 months.

Table 1: Description of respondents to National Health Interview Survey (NHIS) 2015 & 2016 with HPV Vaccination (n=66,700).

Variables

N

%

Sex

Male

30,062

45.1

Female

36,638

54.9

Marital Status

Married

28,373

42.5

Others

34,194

51.3

Race

White-American

52,355

78.5

African-American

8,358

12.5

AI/AN

749

1.1

Asian

3,653

5.5

Multiple Race

1,386

2.1

Region

Northeast

11,170

16.7

Midwest

14,447

21.7

South

23,133

34.7

West

17,950

26.9

Change of Health Insurance

Yes

1,278

1.9

Change Health care place past 12 months

Yes

5,079

7.6

Hepatitis B vaccine

Yes

17,680

26.5

Hepatitis A vaccine

Yes

8,710

13.1

Ever Received HPV shot

Yes

3,999

6

Pap-Smear test past 12 months

Yes

15,368

23

 

Age

Mean±SD

Min-Max

50.35±18.497

18-85

The Table 2 compares the characteristics of people who ever received the HPV vaccination and those who did not. A higher rate of HPV vaccination was found among female vs male p=<0.01(80.2% vs 19.8%). Unmarried (Other marital category [widowed, divorced, separated]) were getting higher rate of HPV vaccination compared to married p=<0.01(74.2% vs 25.8%), with average age (27.42 ± 8.90 SD) that ranged from 18-85 years. In addition, regarding the zone of residence, a high proportion of residents from the South p=<0.01(31.0%) reported having received the HPV shot compared to 20.8% from the Midwest, and 19.1% from the Northeast. Furthermore, those who received HPV vaccination had the higher rate of hepatitis B vaccination (67.2% vs 31%, p=<0.01). Similarly, those who received HPV vaccination recipients also received higher frequency of hepatitis A vaccination (43% vs 15.1%, p=<0.01). Furthermore, the recipients had HPV vaccination 10% higher percent of pap-smear tests done during past 12 months 60.6% vs 50.7%, p=<0.01).

Table 2: Comparing Socio-demographic Characteristics of Female Participants in National Health Interview Survey (NHIS) 2015 & 2016, by history of HPV Vaccination (n=66,700).

Variables

HPV+ n (%)

N=66,700

HPV- n (%)

N=66,700

P value

Sex

Male

793 (19.8%)

20,619 (48.4%)

<0.01

Female

3,206 (80.2%)

22,002 (51.6%)

 

Marital Status

Married

914 (25.8%)

19,351 (49%)

<0.01

Others

2,630 (74.2%)

20,170 (51%)

 

Race

White-American

2,979 (74.8%)

33,021 (77.7%)

<0.01

African-American

586 (14.7%)

5,515 (13%)

 

AI/AN

65 (1.6%)

524 (1.2%)

 

Asian

211 (5.3%)

2,501 (5.9%)

 

Multiple Race

142 (3.6%)

915 (2.2%)

 

Region

Northeast

764 (19.1%)

6,722 (15.8%)

<0.01

Midwest

833 (20.8%)

9,254 (21.7%)

 

South

1,241 (31.0%)

14,925 (35%)

 

West

1,161 (29%)

11,720 (27.5%)

 

Change of Health Insurance

Yes

114 (23.1%)

920 (28.3%)

<0.01

Change Health care place past

12 months

 

 

 

Yes

493 (14.7%)

3,255 (9.1%)

<0.01

Hepatitis B vaccine

Yes

2,463 (67.2%)

12,336 (31%)

<0.01

Hepatitis A vaccine

Yes

1,438 (43%)

5,886 (15.1%)

<0.01

Pap-Smear test past 12 months

Yes

1,938 (60.6%)

11,103 (50.7%)

<0.01

 

Age

Mean±SD

Mean±SD

 

27.42±8.909

43.64±12.884)

The unadjusted and adjusted logistic regression models are shown in the Table 3. The unadjusted modeling for gender signifies that female respondents were significantly more likely (3.79, 95% CI 3.49-4.10) to get HPV vaccination than males. Considering married participants as reference category, unmarried (other marital categories [widowed, divorced, and separated]) were less likely to be vaccinated for HPV (0.36, 95%CI 0.34-0.39). Asians were less likely to get HPV vaccination 1.07; 95% CI 0.92-1.24) compared to White-American (0.85, 95%CI 0.77-0.93) and multiple race considered as a reference category (OR=1). Furthermore, respondents from Northeast (0.87, 95%CI 0.79-0.96) were less likely to be vaccinated for HPV than Midwest (1.10, 95%CI 1.00-1.2), South (1.19, 95%CI 1.09-1.29), and West used as a reference category. In addition, those who changed their health insurance plan were more likely to get HPV vaccination (1.31, 95%CI 1.04-1.63). Those who received hepatitis B vaccination were less likely to get HPV vaccination (0.21, 95%CI 0.20-0.23), this is similar with hepatitis A (0.23, 95%CI 0.22-0.25). Furthermore, those who are at the average age ranged from 18-85 years were more likely getting HPV vaccination (1.13, 95% CI 1.13-1.14).

Table 3: Adjusted and Un-Adjusted Odds Ratio for HPV Vaccination of Female Participants in National Health Interview Survey (NHIS) 2015 & 2016 (n=66,700).

Variables

Un-Adjusted OR (95% CI)

Adjusted OR (95% CI)

Sex

Male

1

1

Female

3.79 (3.49-4.10)

3.84 (2.74-5.39)

Marital Status

Married

1

1

Others

0.36 (0.34-0.39)

0.65 (0.47-0.89)

Race

White-American

0.85(0.77-0.93)

1.00 (0.66-1.52)

African-American

0.73 (0.56-0.94)

1.29 (0.22-7.56)

AI/AN

1.07 (0.92-1.24)

1.34 (0.76-2.37)

Asian

0.58 (0.48-0.69)

1.51 (0.68-3.31)

Multiple Race

1

1

Region

Northeast

0.87 (0.79-0.96)

0.92 (0.59-1.45)

Midwest

1.10 (1.00-1.2)

0.94 (0.63-1.41)

South

1.19 (1.09-1.29)

0.99 (0.68-1.42)

West

1

1

Change of Health Insurance

Yes

1.31 (1.04-1.63)

0.90 (0.65-1.25)

Hepatitis B vaccine

Yes

0.21 (0.20-0.23)

0.47 (0.33-0.65)

Hepatitis A vaccine

Yes

0.23 (0.22-0.25)

0.44 (0.32-0.61)

Age

1.13 (1.13-1.14)

1.12 (1.11-1.15)

These factors were then entered in the multivariate logistic regression model. Results show that compared to males, female odds for the HPV vaccination uptake was 3.84 times higher (95% CI 2.74 5.39). In addition, unmarried (other marital category participants [widowed, divorced, and separated]) were less likely to get the HPV vaccination (0.65, 95%CI 0.47-0.89) compared to married. Similarly, those who received hepatitis B vaccinations were less likely to get the HPV vaccination (0.47, 95%CI 0.33-0.65), and those who received hepatitis A vaccinations (0.44, 95%CI 0.32-0.61). Furthermore, those who are at the average age ranged from 18-85 years were more likely to receive the HPV vaccination (1.12, 95% CI 1.11-1.15).

Discussion

In this study, we observed the majority of participants who reported receiving HPV vaccine were female, white-American, other marital category and from the South. Most participants we have found were White-American married females who resided in the South region, with an average age ranging from 18-85 years. Among the 66,700 respondents, only 6% received the HPV vaccination. An unadjusted logistic regression model for gender signifies that other White-American married females were significantly more likely to get the HPV vaccination than males. After adjusting for potential confounders, race did appear to be associated with the vaccination.

The final model of this study is that the HPV vaccination rate of White-American married females who have received the HPV vaccination is 74.8% than previous study. These findings are in agreement with similar studies on HPV vaccine uptake among White American population, this study reported that 65% of white young women (n=11) completed the 3-dose series of HPV vaccination [13]. There is 10% increase rate of HPV vaccination in the current study. In addition, the previous study findings on HPV vaccination status among female college students have also demonstrated that White American females who were receiving the HPV vaccine were (40.5%) [1]. The current study which is reported receiving HPV vaccine were female (80.2%). There is 40% increase rate of female participants in the current study.

The HPV vaccination is most effective if administered before becoming sexually active. In 2010, 27% of females and 28% of males aged 15-17 years old reported initiating sexual intercourse [11,14,15]. As a result, parents (and future parents) must understand, while not all young adolescents are engaging in sexual activity, administering the vaccine should occur well before any sexual encounter to maximize the protective benefits. In addition to administering the vaccine prior to the first sexual encounter, the American Academy of Pediatrics recommends initiating the 3-dose series in adolescents aged 11 12 years old because of the optimal immune response in younger children [11]. By targeting potential parents early on, knowledge of vaccine benefits and safety will be inherent when making informed decisions on whether and when, regardless of age, future daughters should receive the HPV vaccine.

According to Health Belief Model and Theory of Planned Behavior [5,11,13], parents and their children have the potential to address these attitudes and beliefs regarding the HPV vaccine. Additionally, public health officials can encourage those supporting the HPV vaccine mandate to advocate to representatives and policy makers to ensure the health of future generations is protected against HPV infections.

The final finding of this study is that African-American were less likely to receive the HPV vaccination compared to White-American females. Similarly, AI/AN and multiple races are less likely to receive the HPV vaccination compared to White-American females. Therefore, we must increase the HPV vaccination rates among African-American, AI/AN, and multiple races by allocating resources, recommendations of HPV vaccination at every visit. Improve and development of nationwide vaccination standard and affordable price for HPV vaccine to deal with health insurance companies and also with stakeholders.

Strength

The broad sample size (n=66,700) is considered to be a strength of this study including the participants are from different regions such as Northeast, Midwest, South, and West in the United States

Limitations

This study has some limitations. First, unclear data variables include dosage of vaccine and number of HPV shots, and age at first received vaccine. Second, there is the possibility of self-report biases even though NHIS data collection techniques are designed to limit reporting biases. Self-reporting bias may arise due to the individual not remembering previous HPV vaccination or the individual refuses to answer due to the stigma and possible discrimination associated with HPV infection.

Finally, this study looked at only a few sociodemographic characteristics for the HPV vaccination uptake. The information is related to change in health insurance plans, hepatitis A and hepatitis B vaccines received, marital status, sex, age, race, and region. The importance of the HPV vaccination, the number of HPV vaccinations and the age at first vaccine received should be gathered in the future NHIS surveys.

Conclusion

The purpose of our study was to examine the uptake rate of the HPV vaccination among White-American females. In this study, we examined married and other marital category females because they are a unique population. Our findings show the greatest indicators of vaccinating participants were White-American females, rather than African-American, AI/AN, and multiple races. As evidenced in our findings, the majority of female participants 54.9% believed that vaccinations against HPV helped to avoid negative health outcomes such as genital warts and various cancers. The final model of this study is that White-American married females who have received the HPV vaccination were 3.84 times higher. This study did not focus towards male populations and did not assess intentions for vaccinating males, which is an area in need of more research. However, these findings, in addition to emerging evidence on HPV vaccine uptake.

Acknowledgment

This study was supported by Dr. Shayesteh Jahanfar, Dr. Jeff Inugnu, and Dr. Neli Ragina. School of Health Sciences and CMU college of Medicine, Central Michigan University. The data reviewed from the National Health Interview Survey (NHIS) 2015 & 2016.

References

1. Daley EM, Vamos CA, Buhi ER, Kolar SK, McDermott RJ, Hernandez N, et al. Influences on human papillomavirus vaccination status among female college students. J Womens Health (Larchmt). 2010; 19: 1885-1891.

2. Friedman AL, Shepeard H. Exploring the knowledge, attitudes, beliefs, and communication preferences of the general public regarding HPV: findings from CDC focus group research and implications for practice. Health Educ Behav. 2007; 34: 471-485.

3. Crosby RA, DiClemente RJ, Salazar LF, Nash R, Younge S, Head S. Human papilloma virus vaccine intention among college men: what’s oral sex got to do with it? J Am Coll Health. 2012; 60: 8-12.

4. Donadiki EM, Jimenez-Garcia R, Hernandez-Barrera V, Carrasco-Garrido P, López de Andrés A, Jimenez-Trujillo I, et al. Knowledge of the HPV vaccine and its association with vaccine uptake among female higher-education students in Greece. Hum Vaccin Immunother. 2013; 9: 300-305.

5. Pierre Joseph N, Clark JA, Mercilus G, Wilbur M, Figaro J, Perkins R. Racial and ethnic differences in HPV knowledge, attitudes, and vaccination rates among low-income African-American, Haitian, Latina, and Caucasian young adult women. J Pediatr Adolesc Gynecol. 2014; 27: 83-92.

6. Wilson KL, White A, Rosen BL, Chiappone A, Pulczinski JC, Ory MG, et al. Factors Associated with College Students’ Intentions to Vaccinate Their Daughters Against HPV: Protecting the Next Generation. J Community Health. 2016; 41: 1078-1089.

7. Tan W, Viera AJ, Rowe-West B, Grimshaw A, Quinn B, Walter EB. The HPV vaccine: are dosing recommendations being followed? Vaccine. 2011; 29: 2548-2554.

8. Baker JL, Leader AE, Voytek CD, Brawner BM, Peters N, Silverman R, et al. Perspectives on human papillomavirus (HPV) vaccination among African American female adolescents. American Journal of Health Studies. 2012; 27: 204.

9. Kurdgelashvili G, Dores GM, Srour SA, Chaturvedi AK, Huycke MM, Devesa SS. Incidence of potentially human papillomavirus-related neoplasms in the United States, 1978 to 2007. Cancer. 2013; 119: 2291-2299.

10. Gelman A, Miller E, Schwarz EB, Akers AY, Jeong K, Borrero S. Racial disparities in human papillomavirus vaccination: does access matter? J Adolesc Health. 2013; 53: 756-762.

11. Beavis AL, Levinson KL. Preventing Cervical Cancer in the United States: Barriers and Resolutions for HPV Vaccination. Front Oncol. 2016; 6: 19.

12. Spencer AM, Brabin L, Roberts SA, Patnick J, Elton P, Verma A. A qualitative study to assess the potential of the human papillomavirus vaccination programme to encourage under-screened mothers to attend for cervical screening. J Fam Plann Reprod Health Care. 2016; 42: 119-126.

13. Buchwald D, Muller C, Bell M, Schmidt-Grimminger D. Attitudes toward HPV vaccination among rural American Indian women and urban White women in the northern plains. Health Educ Behav. 2013; 40: 704-711.

14. Brewer NT, Fazekas KI. Predictors of HPV vaccine acceptability: a theory-informed, systematic review. Prev Med. 2007; 45: 107-114.

15. Sadry SA, De Souza LR, Yudin MH. The impact of ethnicity on awareness and knowledge of and attitudes towards the human papilloma virus and vaccine among adult women. J Obstet Gynaecol Can. 2013; 35: 995-1003.

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Measles was a leading cause of infant and child morbidity and mortality in Oman before the introduction of measles vaccine by 1975 and thereafter until 1994. With the introduction of a second dose of measles vaccine in 1994, coverage for first and second doses of measles vaccine increased more than 95% in 1996 and has been sustained at a level greater than >95% since then. A national Measles and Rubella (MR) immunization catch-up campaign targeting children ages 15 months to 18 years was conducted in 1994 that achieved 94% coverage. As a result, the incidence of measles has declined markedly in recent years, to ≤ 1 case per million persons in 2012 and to zero cases in 2013.

Oman has made significant progress toward measles elimination and has met the regional elimination goals. However, new challenges faced by Oman, for instance with increased globalization, has led to issues such as outbreaks from imported cases. Additional challenges still remain with regard to increasing identification and immunization of unvaccinated non-Omani workers and their families.

Salah T Al Awaidy1*, Said Al Baqlani2 , Salim Al Mahrouqi3 , Badder Al Rawahi3 , Suleiman Al Busaidi1 , Idris Al Obaidani3 , Maryam Al Shabibi3 , Hosammudin Mohammed NwarAl Den3 , Adil Mohammed Al Barwani4 , Aisha Said Al Amri and Nadia Teleb5


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Avian Influenza Type A-H5N1 Epidemiological Model: Puerto Rico as a Case Study

Our research focused on Avian Influenza Type A-H5N1, specifically on an epidemiological model centered in Puerto Rico. Our main goal is to address the following: first, to determine the potential outbreaks of this disease in Puerto Rico using as a base the location of the poultry industry as a hub, we are interested in the repercussions of the infection among the human-to-human potential interaction. The second goal centers on the possibility of vaccination to mitigate an epidemic among humans. In order to address these goals and future ones, we will construct a mathematical model and use parameters according to two cases; the first is a single population model and the second one is a metapopulation model involving 5 cities in Puerto Rico. Our research will specifically target the spread of this particular disease, to investigate possible alternatives to mitigate the spread using measures of immunization. Our results show that a 30% vaccination regime will eradicate the disease in cities that are immunized.

Collazo-Rivera M and Cruz-Aponte M*


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Schistosome Immunomics: High-Throughput Vaccine and Diagnostic Antigen Discovery

Schistosomiasis remains one of the highly prevalent and serious helminthiases in the countries of Asia, Africa and Latin America. Despite the accessibility of an effective drug against the fatal parasites, drug-based treatment projects still have certain limitations and it is likely that vaccine and effective diagnostic tools are essential for schistosomiasis control. Despite the several decade vaccine development has witnessed the finding and testing of couple of candidate targets, none have shown satisfactory protection. Upon the coming of genome era, it has revolutionized the study of the drug, vaccine, and immunodiagnosis, and also catalyzed a switch from traditional manual testing to automation operation.

Yang Guo, Bei Li, Xuzhi Ruan, Zongyun Chen and Jian Li*


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Vaccination Coverage and Sustaining Control of Measles in Africa: A Global Health Perspective

For over 50 years, a safe, effective and inexpensive vaccine has been in use but several challenges continue to hamper universal coverage and the sustained control of measles. Before the year 2000, measles was killing over 700,000 children each year worldwide of which 60% occurred in Sub-Saharan Africa [1]. Epidemiologic reports showed that although an estimated 15.6 million deaths had been prevented by measles vaccination between 2000 and 2013, progress has stalled and previous gains are being reversed [2]. Measles related deaths vary depending upon the average age of infection, the nutritional status of the population, measles coverage, HIV infection, vitamin A deficiency and access to health care [3]. The death rate due to measles is so high in Africa that, on average, a child dies every minute. To make the matter worse, every person with measles has a 90% chance of infecting people with whom they come into close contact, if they are unvaccinated [1]. Yet a single dose of measles vaccine is proven to be 93% effective at preventing disease in vulnerable populations exposed to the virus at a relatively low cost ($1 US dollar). The fact that many lives are still lost to this vaccine-preventable virus remains a key concern for global health.

Olivia G Mendel1 , Stephanie K King1 and Juliet N Sekandi2*


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Nanovaccine Delivery Systems in Vaccine Formulations

The important biological molecules such as polysaccharides, proteins, allergens and Pathogen Associated Molecular Patterns (PAMPs) are of nanometer in size. Hence, the size, charge, hydrophobic properties will influence their effects on the immune system by way of specific and varied response. Vaccines play a pivotal role in disease containment and prevention. One of the bottle necks is the vaccine administration system. Earlier vehicles and adjuvant systems pose unwanted reactions due to the nature of delivery system used in the vaccine. Delivery systems are those materials used for the administration of vaccines s in a controlled manner aimed to achieve a therapeutic effect. These systems provide: cell or tissue targeted delivery of the antigen, improved antigen presentation, solubility, sustained release and protection of the prophylactic agent from degradation.

Aruni Wilson1*


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Therapeutic Vaccination against Cancers - A Conceptual Overview with Updates on the Immunological Approach

Cancer immunotherapy has now finally made its way and entered a new era, after decades of intensive searching of a cure for the incurable. Current attentions are particularly drawn by the very promising outcomes from a series of experimental and clinical studies recently concluded [1], having tested and verified the “Immune Checkpoint Blockade” working hypothesis initially proposed by Dr. James Allison nearly 20 years ago [2]. The next central question is about how to extend or maximize the therapeutic and survival benefits for greater numbers of patients, and of different cancer types. This may be achieved by further identifications of new target checkpoint inhibitors, emphasizing more on the tumor-specific antigenic signals, and through combination with the therapeutic vaccination approach in particular. Here, by joining in the discussion, I intend to start with direct reference to various basic yet constantly evolving concepts based on which vaccination against neoplasm has been developed along, and now progressing towards.

Huang FP1*


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Evaluation of a Polyvalent Vaccine Obtained From Divergent Low Pathogenic H5N2 Isolates of the Avian Influenza Virus in Mexico

In Mexico, the strategy used for controlling the Avian Influenza Virus (AIV) involves the use of immunizations through an inactivated emulsion vaccine (H5N2), which protects birds from the disease. It has been shown that the strain used in this vaccine is phylogenetically distant from the strains that are isolated in the field. Therefore, the goal of this study was to prepare and evaluate a polyvalent vaccine with genetically divergent isolates of the low-pathogenicity H5N2 avian influenza virus strains that are prevalent in Mexico. A polyvalent vaccine (Poly-AI) was prepared using five isolates that exhibited phylogenetic divergence from the low-pathogenicity avian influenza H5N2 virus strains found in Mexico. Chickens were immunized with Poly-AI and challenged 28 days post-vaccination with two Low Pathogenic Avian Influenza Virus (LPAIV) isolates contained in the vaccine and one High Pathogenic Influenza Virus (HPAIV). Serology was done at different times and clinical signs were recorded. This is the first study that documents the degree of pathogenicity differences between various isolates that exhibit genetic variation in the nation. The experimental Poly-AI vaccine eliminated the clinical signs of the disease, demonstrated 100% protection against the challenge with a highly pathogenic strain and decreased excretion when challenged with homologous and high virulence strains, which was detected by qRT-PCR.

Elia Armas Bojórquez1 , Edith Rojas Anaya1 , Gary García Espinosa2 , Fernando Diosdado Vargas1 and Elizabeth Loza-Rubio1*