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VACCINES
WHAT EVERYONE NEEDS TO KNOW®
VACCINES
WHAT EVERYONE NEEDS TO KNOW®
KRISTEN A. FEEMSTER
1
3
Oxford University Press is a department of the University of Oxford. It furthers
the University’s objective of excellence in research, scholarship, and education
by publishing worldwide. Oxford is a registered trade mark of Oxford University
Press in the UK and certain other countries.
“What Everyone Needs to Know” is a registered trademark
of Oxford University Press.
Published in the United States of America by Oxford University Press
198 Madison Avenue, New York, NY 10016, United States of America.
© Oxford University Press 2018
All rights reserved. No part of this publication may be reproduced, stored in
a retrieval system, or transmitted, in any form or by any means, without the
prior permission in writing of Oxford University Press, or as expressly permitted
by law, by license, or under terms agreed with the appropriate reproduction rights
organization. Inquiries concerning reproduction outside the scope of the above should
be sent to the Rights Department, Oxford University Press, at the address above.
You must not circulate this work in any other form
and you must impose this same condition on any acquirer.
Library of Congress Cataloging-in-Publication
Data Names: Feemster, Kristen A., author.
Title: Vaccines : what everyone needs to know / Kristen A. Feemster.
Description: New York, NY : Oxford University Press, [2017] |
Includes bibliographical references and index.
Identifiers: LCCN 2017033339| ISBN 9780190277901
(hardcover : alk. paper) | ISBN 9780190277918 (paperback : alk. paper)
Subjects: LCSH: Vaccination—Popular works. |
Vaccination—History. | Vaccines.
Classification: LCC RA638 .F44 2017 |
DDC 614.4/7—dc23
LC record available at https://lccn.loc.gov/2017033339
This material is not intended to be, and should not be considered, a substitute for
medical or other professional advice. Treatment for the conditions described in this
material is highly dependent on the individual circumstances. And, while this material
is designed to offer accurate information with respect to the subject matter covered
and to be current as of the time it was written, research and knowledge about medical
and health issues is constantly evolving and dose schedules for medications are being
revised continually, with new side effects recognized and accounted for regularly.
Readers must therefore always check the product information and clinical procedures
with the most up-to-date published product information and data sheets provided by
the manufacturers and the most recent codes of conduct and safety regulation. The
publisher and the authors make no representations or warranties to readers, express
or implied, as to the accuracy or completeness of this material. Without limiting the
foregoing, the publisher and the authors make no representations or warranties as to
the accuracy or efficacy of the drug dosages mentioned in the material. The authors
and the publisher do not accept, and expressly disclaim, any responsibility for any
liability, loss or risk that may be claimed or incurred as a consequence of the use and/
or application of any of the contents of this material.
1 3 5 7 9 8 6 4 2
Paperback printed by LSC Communications, United States of America
Hardback printed by Bridgeport National Bindery, Inc., United States of America
With love to James and our sunshines, TE and FM.
In memoriam to Mom, my greatest superhero.
CONTENTS
ACKNOWLEDGMENTS xv
ABBREVIATIONS xvii
INTRODUCTION xix
What is an antigen? 2
What happens when the immune system is confronted by an antigen? 2
How do cells signal each other in the process of creating antibodies? 3
Which is better, natural immunity or immunity after vaccination? 3
What is the real risk of vaccine-preventable diseases? 4
What is herd immunity? 5
What happens when immunization rates are not high enough to
achieve herd immunity? 6
How large are most outbreaks? 6
What is the difference between immunization and vaccination? 7
What are the different types of vaccines? 7
Why are there so many types of vaccines? 9
Why do most vaccines require more than one dose? 10
Besides antigens, what else are vaccines made of? 10
Even if these substances are necessary, are they safe? 12
viii Contents
3. Vaccine Development 31
5. Vaccine Safety 69
APPENDIX 155
SELECTED BIBLIOGRAPHY 167
INDEX 175
ACKNOWLEDGMENTS
What is an antigen?
Antigens are proteins on the surface of a pathogen that prompt
the production of antibodies by the immune system. Bacteria
and viruses are both covered in antigens, and during the proc-
ess of natural infection, these antigens are what the body rec-
ognizes. Depending on the pathogen, its antigen coating can
be made up of several proteins or several thousand.
Vaccines, on the other hand, are often made using just a
few antigens from a bacteria or virus. This is because some
antigens are better than others at sparking the immune sys-
tem. This is also because it is important to separate the parts
of a pathogen that cause disease and make one sick from those
that induce an antibody response. The ability to cause disease
is called virulence, whereas the ability to induce a protective
immune response is called immunogenicity.
The number of antigens in vaccines is actually quite small
compared to the number of antigens that confront the immune
system during an actual infection (or just from the environ-
ment on a daily basis). For example, the pathogen that causes
whooping cough contains more than 3,000 antigens; the vac-
cine that is used to protect against whooping cough contains
only 3–5 different antigens. Our immune systems are stimu-
lated all the time, but all stimulation is not the same.
five different proteins that are either toxins or are part of the
bacteria itself (compared to the 3,000 proteins contained in a
whole pertussis bacterium). The inactivated proteins cannot
cause infection or disease, but they will lead to an immune
response to recognize and inactivate the bacteria or toxin when
actual infection occurs.
Similar to protein subunit vaccines for bacteria, recombinant
vaccines are made from individual viral proteins that are known
to induce a protective immune response. To make recombinant
vaccines, the gene that is responsible for making the selected
protein is inserted into the DNA of a yeast cell. As the yeast
reproduces, so too does the DNA, and the resulting protein is
purified to make a vaccine. Both hepatitis B and HPV vaccines
are made using this technique.
Polysaccharide vaccines target a certain group of bacteria that
have a special capsule on their surface made of sugars or poly-
saccharides. Because their capsule is what the body interacts
with first, it is also what the immune response targets. Thus,
vaccines for encapsulated bacteria are made using this capsule
rather than any proteins from the bacteria.
However, polysaccharide capsules do not induce immune
memory well, nor do they work well in children younger
than age 2 years. This is a problem because the bacteria with
capsules— pneumococcus, meningococcus, and Haemophilus
influenzae b (Hib)—can cause severe disease in young children.
This led to the development of conjugate vaccines, in which the
polysaccharide capsule is attached to a protein that is able to
turn on memory cells.
What is inoculation?
The Merriam–Webster Dictionary defines inoculation as “the
introduction of a pathogen or antigen into a living organism
to stimulate the production of antibodies.” During the 1721
smallpox epidemic, fluid from an infected individual’s small-
pox pustule was introduced to healthy individuals through a
small cut in the skin. The person who received the inoculation
would develop smallpox but generally a milder case. The indi-
vidual would then be protected from subsequent infections
through antibody protection, although the role of antibodies
was not understood at the time.
The introduction of inoculation was fraught with contro-
versy. Cotton Mather, a Boston minister known for his cham-
pioning role in the Salem witch trials, made the first call for
inoculation in response to the 1721 epidemic.
Mather first learned of inoculation and its benefits from both
incoming slaves who had the procedure performed in their
home country and texts from the Royal Society of Medicine in
Britain. Mather had previously portrayed smallpox in religious
terms—an act of Providence or a reflection of man’s sin—but
during the 1721 epidemic, he chose instead to intervene, citing
the will of God.
Interestingly, Mather found almost no support within the
medical community, save for one physician named Zabdiel
Boylston, who agreed to offer inoculation. By the end of the
epidemic, Boylston had inoculated 248 patients, mostly in
secret. However, by the time the next smallpox epidemic hit
Boston in 1730, the practice was beginning to gain traction.
A Brief History of Vaccines 19
that she never got smallpox because she had been exposed to
cowpox, a viral disease similar to smallpox but milder and less
common. Cowpox was mostly limited to farmworkers who
acquired the disease through cow udders. It was not as severe
as smallpox, but it still caused inflamed joints, skin ulcers,
fever, and limb pain. As opposed to smallpox, cowpox did not
cause disfigurement or death.
Jenner’s first field experiment was to find a group of farm-
ers who had a history of cowpox and inoculate them with
smallpox; he did so, and none of the farmers developed small-
pox. In May 1796, he performed the ultimate test: He took fluid
from lesions of a milkmaid who had just developed cowpox
and then inoculated a young boy with it. Several weeks later,
Jenner inoculated the boy with smallpox and nothing hap-
pened; the boy never showed symptoms of the more serious
disease. Jenner had demonstrated that cowpox gave immunity
against smallpox. By 1801, 100,000 people throughout Europe
had received the first cowpox-based smallpox vaccine.