Has your neurologist discussed HPV vaccination with you?

What to advise MSers about the HPV vaccine?



You may be aware that for almost a decade young girls living in the UK have been offered the HPV vaccine at ~12-14 years of age. The HPV vaccine is to prevent infection with the sexually transmitted human papillomavirus (HPV) that is known to cause cervical cancer and several other cancers. The current issue is that innovation never stands still, technology moves on and society changes its behaviour. All of these are coming together to create a perfect storm that has major implications for MSers. 


The innovation: The current NHS funded vaccine (Gardasil) covers only 4 strains of HPV and reduces the risk of cervical cancer by ~67%. The newer more advanced HPV vaccine covers 9 HPV strains and reduces the risk of cervical cancer by over 90%. The problem is the Department of Health are not yet prepared to pay for the more expensive vaccine that covers 9 strains. It is important to realise that the newer vaccine also covers more strains of HPV that cause warts, in particular, genital warts. Is this important? Yes, it is. If you decide to go onto an immunosuppressive therapy, in particular, an immune reconstitution therapy or IRT, then suppression of your immune system allows the virus to escape and to start replicating. I am aware of two cases at other centres who have had alemtuzumab only to see their genital warts become a major problem. I am also aware of a patient who developed a problem when her common old garden variety of cutaneous warts spread post-alemtuzumab. These anecdotal cases are very important and I now view warts, be they genital or cutaneous, as a relative contraindication to IRTs, particularly the non-selective IRTs such as alemtuzumab and HSCT. 


Social changes: There are public health issues that are as relevant to MSers as the general population. HPV is not only a problem for women. HPV is a well-established cause of penile and anal cancer and causes a small proportion of throat and oesophageal cancers. Therefore it makes sense for males to be vaccinated against HPV as well. In the UK boys who have sex with boys and are prepared to admit it can have the HPV vaccine. But what about men? The rationale for targeting the general population is to reduce the pool of susceptible people and thereby reduce the spread of the virus. Epidemiologists call the latter herd immunity. For herd immunity to be effective you typically need over 90% of the population to vaccinated.


The epidemiology of HPV infection is also changing. People are becoming infected later in life and are spreading the virus. Social media and dating apps have revolutionised the dating world and many older people are becoming promiscuous in older age and are having unsafe sex. As a result of this, there has been a large increase in the incidence of sexually transmitted diseases in older people, including HPV infections. This has prompted some commentators to suggest that public health officials extend the HPV vaccine to all women and possibly all men. Why wouldn’t you want to reduce your risk of getting cervical cancer? Isn’t prevention better than having to treat HPV infection and its downstream effects, i.e. premalignant cervical lesions or cervical cancer?


As a result of these trends, an increasing number of MSers are asking about the HPV vaccine. Similarly, when I go to meetings neurologists are asking me for advice or what to do about vaccines, in particular, the HPV vaccine There are several questions that HPV vaccination raises that are directly relevant to MSers.


Question 1: If I have been vaccinated with the older quadrivalent vaccine could I receive the new vaccine to cover the other strains of the virus?


Yes, there is data that shows that the previous vaccination against HPV doesn’t stop your immune system from responding to the components cover the new strains.


Question 2: As I am on a DMT can I have the HPV vaccine?


This all depends on the DMT you are on. For the non-immunosuppressive immunomodulators such as interferon-beta and glatiramer acetate vaccination is not a problem. These agents do not blunt immune responses to vaccines. For the other DMTs to story is not that clear. Fingolimod and ocrelizumab are known to blunt vaccine responses. Vaccine responses to component vaccines on dimethyl fumarate have been studied and were normal. However, I am not aware of any specific studies looking at the HPV vaccine. I would, however, think it would be fine to receive the HPV vaccine if you are on DMF. Teriflunomide is similarly unlikely to blunt the immune response to HPV, but we don’t have specific data on the HPV vaccine and teriflunomide Natalizumab mode of action is unique and is unlikely to affect peripheral immune responses. For the IRTs (alemtuzumab, cladribine, mitoxantrone and HSCT) vaccination should be delayed until after immune system reconstitution.


Question 3: I need to start a DMT, but I want to have the HPV vaccine or extend my cover with the new polyvalent vaccine, how long will I need to wait before I can start treatment?


The polyvalent vaccine at the moment requires 2 or 3 doses with the last dose given at 5 or 6 months. Ideally, to give your immune system a chance to respond to the vaccine you will need to wait until 4 weeks after the final booster, i.e. 6 or 7 months.


Question 4: Should I delay starting DMTs to have the vaccine?


There is no simple answer to this question. You have to balance the risks and benefits of having the vaccine against the risks of untreated MS. In relation to the IRTs, I would suggest going ahead and starting the IRT and delaying the vaccine until you have reconstituted your immune system. Delaying starting an IRT to have the vaccine does not make immunological sense in that the memory responses you have just made to the vaccine could potentially get depleted and depending on the intensity of the immunodepletion may not recover. For maintenance DMTs, in particular, fingolimod, dimethyl fumarate and ocrelizumab, you should probably delay starting treatment to have the vaccine.


Question 5: If I want the new polyvalent vaccine will the NHS cover it?


At present, the answer is no. Public Health England cover the quadrivalent vaccine under the national vaccine programme. If you want to be vaccinated against HPV you will have to cover the costs of the vaccine yourself. This is not too dissimilar to what happens with travel vaccines.


As you can see HPV vaccination is one of those factors that have to be put in the mix when deciding which is the correct DMT for you. It is not a major factor but is an important factor nevertheless. At the moment I don’t routinely advise my patients on this topic, but it is something that has future health implications, be they sexual, so maybe we need to do this routinely. What is your view on this? Do you think healthcare professionals should be obliged to discuss issue around vaccination before the start of a DMT?

CoI: multiple

The consequences of Britain’s heatwave for MSers is profound

 

How are you tolerating the heat? One patient after another in my MS clinic yesterday complained about heat sensitivity, worsening fatigue, pseudo-relapses (heat-induced intermittent symptoms) and difficulty sleeping. How are you coping; do you have any advice for your fellow MSers?
 
London feeling the effects of global warming.



Please note that the main consequences of a raised body temperature in demyelinated, or remyelinated, pathways is slowed conduction. The commonest example is exercise-induced fatigue, but this summer’s heatwave is causing symptoms without the need for exercise. Some MSers are finding walking difficult; their legs begin to drag minutes into walking rather than after 20-30 minutes. One patient has noticed blurring of vision mid-morning when in the past this would only happen in the late afternoon. The reason for this is that those demyelinated segments in the nerve stop conducting due to conduction block induced by a slight rise in temperature affecting the functioning of the sodium channels. These are the molecules in the membranes of nerve cells that transmit the electrical signal down a nerve fibre, which require energy to work. These ion pumps are optimised to function at a certain temperature and explains why MSers are heat sensitive.

I assume you have heard of Uhthoff’s phenomenon. Wilhelm Uhthoff (1853-1927) was a famous German Professor of ophthalmology who described temporary visual loss associated with optic neuritis linked to physical exercise. This was later found to be caused by a rise in body temperature. This phenomenon is now known to affect other neurological systems as well; for example, the motor system when walking, balance and sensory pathways and even the cognitive centres.

Apart from cooling, we have not had a treatment for Uhthoff’s phenomenon. More recently the drug Fampridine has been licensed to improve walking speed in MSers. Interestingly one of the patients I saw yesterday volunteered that since starting fampridine a few weeks ago his heat sensitivity had improved.

 
 

Goodman et al. Sustained-release oral fampridine in multiple sclerosis: a randomised, double-blind, controlled trial. Lancet. 2009 Feb 28;373(9665):732-8.

Symptomatic treatments and behavioural & environmental therapy (cooling) have been the mainstay of treating MS-related heat sensitivity. Having a drug to treat conduction block is, therefore, welcomed. However, I remain sceptical about their long-term effectiveness which is why we need effective remyelination therapies. Remyelination therapies should also be neuroprotective preventing or slowing down the degeneration of nerve fibres that have been left vulnerable by demyelination.

CoI: Multiple

Research: fingolimod after natalizumab keeps relapses at bay

 

#MSBlog: How soon after stopping natalizumab (Tysabri) do you start fingolimod (Gilenya)?
 

Epub: Havla et al. Fingolimod reduces recurrence of disease activity after natalizumab withdrawal in multiple sclerosis. J Neurol. 2012.

Background: After discontinuation of natalizumab (Nz), MS disease activity often recurs.

 
“The level of rebound activity can be very severe!”
 
Objective: This study assessed the recurrence of clinical disease activity during the first year after switching from Nz to fingolimod (Fingo) in RRMSers. 
 
Methods: The number of relapses and the annualized relapse rate (ARR) before, during and after Nz discontinuation were determined and compared between 26 MSers who switched to Fingo within 24 weeks, and 10 MSers who remained without disease modifying therapy (therapy free group = TFG). 
 
Results: Median follow-up post-Nz discontinuation was 55.1 weeks. In a subgroup (n = 20), the occurrence of contrast-enhancing-lesions (Gd+) on magnetic resonance imaging (MRI) was determined. Eleven MSers (42 %) in the Fingo group and seven MSers (70 %) in the TFG had one or more relapses after cessation of Nz during follow-up (p < 0.05). One of the 11 (9 %) MSers in the Fingo group and 6/9 (67 %) MSers in the TFG showed Gd+ lesions during follow-up (p < 0.05). MSers who switched to Fingo  ≤ 12 weeks after Nz discontinuation (n = 9) showed a trend for a lower post-Nz ARR compared to MSers who started Fingo therapy >12 weeks after Nz was stopped (n = 17). Most relapses in the Fingo group occurred just before or within 8 weeks after starting Fingo. 
 

Conclusion: These observation suggests that initiation of Fingo treatment after Nz discontinuation reduces the recurrence of disease activity compared to withdrawal without further immunomodulatory treatment. In the Fingo group the ARR tended to depend on the time interval between discontinuation of Nz and initiation of Fingo.“These results support our recent change in practice to limit the washout period when switching from Nz to Fingo. The sooner you switch the greater the likelihood of preventing post-Nz rebound!”

 

Other related posts of interest:
 
01 Dec 2012
“The potential rebound in MS disease activity that is commonly seen after withdrawal of natalizumab, and now fingolimod, reminds me of the book ‘Waiting for the Barbarians’ by JM Coetzee, which I read as a teenager.
27 Jul 2012
Rebound in MS disease activity on fingolimod withdrawal. Epub: Hakiki et al. Withdrawal of fingolimod treatment for relapsing-remitting multiple sclerosis: report of six cases. Mult Scler. 2012 Jul. The objective of this study is to 

19 Feb 2012
Rebound of disease activity after withdrawal of fingolimod (FTY720) treatment. Arch Neurol. 2012;69:262-4. BACKGROUND: The oral sphingosine-1-phosphate receptor modulator fingolimod (FTY720/Gilenya) was recently 

03 Jul 2012
BACKGROUND AND PURPOSE: MSers discontinuing natalizumab are at risk of rebound of disease activity. METHODS: In the present multi-center, open-label, non-randomized, prospective, pilot study, the investigators’ 

31 Oct 2012
Natalizumab dramatically reduces relapses in MSers with active MS, but it may induce progressive multifocal leukoencephalopathy (PML).(1) A rebound of MS or an immune reconstitution inflammatory syndrome (IRIS) were 

30 Oct 2012
Clinical and/or MRI signs suggestive of disease rebound were observed in three MSers.  “These studies and case reports confirm mine and many other neurologists’ observations of rebound on natalizumab withdrawal.

CoI: multiple

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